MA50Remark Code (RARC)Active
Effective 01/01/1997 · Updated 03/01/2014

MA50 Remark Code - Investigational Device or Clinical Trial Number

The MA50 remark code indicates that the claim was denied due to a missing, incomplete, or invalid Investigational Device Exemption (IDE) number or Clinical Trial number. This remark supplements a Claim Adjustment Reason Code that already identifies the primary reason for the adjustment, providing additional specificity regarding the documentation required for the claim.

How It Relates to the Denial

Typically, the MA50 remark code accompanies adjustment reason codes related to claims for services or devices used in clinical trials. The combination of these codes signals that the payer requires proper documentation of the IDE or Clinical Trial number to process the claim correctly.

Common Scenarios

1A provider submitted a claim for a new device used in a clinical trial but did not include the Investigational Device Exemption number.
→ The MA50 remark code is pointing out that the necessary IDE number is missing, which is required for the claim to be considered valid.
2A claim was billed for a clinical trial service, but the Clinical Trial number provided was incomplete.
→ The MA50 remark code indicates that the payer found the Clinical Trial number insufficient, implying the need for a complete and valid number to proceed with processing.
3A facility submitted a claim for a procedure involving an investigational device but received a denial indicating an invalid IDE number.
→ The MA50 remark code highlights that the IDE number submitted with the claim was deemed invalid, necessitating correction before resubmission.

What to Do

  1. Obtain the correct Investigational Device Exemption number or Clinical Trial number and ensure it is complete and valid.
  2. Review the claim documentation to verify that the appropriate numbers are included in the correct fields.

What to Check

  • The claim submission details to confirm the IDE or Clinical Trial number was included.
  • Payer guidelines regarding the requirements for IDE or Clinical Trial numbers on claims.
  • The original documentation submitted with the claim to ensure accuracy and completeness of the required identifiers.