The following data is part of a premarket notification filed by Cardiovascular Diagnostic Services with the FDA for Coag-1 Aptt Test Card.
Device ID | K891015 |
510k Number | K891015 |
Device Name: | COAG-1 APTT TEST CARD |
Classification | Activated Partial Thromboplastin |
Applicant | CARDIOVASCULAR DIAGNOSTIC SERVICES P.O. BOX 14025 2810 MERIDIAN PKWY SUITE 106 Research Triangle Park, NC 27709 |
Contact | Sharon C Dermott |
Correspondent | Sharon C Dermott CARDIOVASCULAR DIAGNOSTIC SERVICES P.O. BOX 14025 2810 MERIDIAN PKWY SUITE 106 Research Triangle Park, NC 27709 |
Product Code | GFO |
CFR Regulation Number | 864.7925 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-02-28 |
Decision Date | 1989-05-22 |