The following data is part of a premarket notification filed by Ortho Diagnostic Systems, Inc. with the FDA for Orthokrome* Antithrombin.
| Device ID | K900400 |
| 510k Number | K900400 |
| Device Name: | ORTHOKROME* ANTITHROMBIN |
| Classification | Antithrombin Iii Quantitation |
| Applicant | ORTHO DIAGNOSTIC SYSTEMS, INC. 1001 U.S. HIGHWAY 202 P.O. BOX 350 Raritan, NJ 08869 -0606 |
| Contact | Gail Kromer |
| Correspondent | Gail Kromer ORTHO DIAGNOSTIC SYSTEMS, INC. 1001 U.S. HIGHWAY 202 P.O. BOX 350 Raritan, NJ 08869 -0606 |
| Product Code | JBQ |
| CFR Regulation Number | 864.7060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-01-29 |
| Decision Date | 1990-03-15 |