The following data is part of a premarket notification filed by Seragen Diagnostics, Inc. with the FDA for Ck/mb Immuno-isoenzyme Control Serum.
Device ID | K840793 |
510k Number | K840793 |
Device Name: | CK/MB IMMUNO-ISOENZYME CONTROL SERUM |
Classification | Enzyme Controls (assayed And Unassayed) |
Applicant | SERAGEN DIAGNOSTICS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | JJT |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-02-23 |
Decision Date | 1984-04-13 |