MYOGLOBIN RIA TEST KIT— 510(k) K915233

Substantially Equivalent

Pro Diagnostics, Inc.

FDA 510(k) clearance K915233 for MYOGLOBIN RIA TEST KIT, Substantially Equivalent on 1992-03-30. Applicant: Pro Diagnostics, Inc..

Clearance details

Applicant: Pro Diagnostics, Inc.
Product code: Code DDR
Advisory panel: Immunology
Date received: 1991-11-22
Decision date: 1992-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.