The following data is part of a premarket notification filed by Pb Diagnostic Systems, Inc. with the FDA for Opus Procainamide Test System.
| Device ID | K934762 |
| 510k Number | K934762 |
| Device Name: | OPUS PROCAINAMIDE TEST SYSTEM |
| Classification | Enzyme Immunoassay, Procainamide |
| Applicant | PB DIAGNOSTIC SYSTEMS, INC. 151 UNIVERSITY AVE. Westwood, MA 02090 |
| Contact | Nancy M Johansen |
| Correspondent | Nancy M Johansen PB DIAGNOSTIC SYSTEMS, INC. 151 UNIVERSITY AVE. Westwood, MA 02090 |
| Product Code | LAR |
| CFR Regulation Number | 862.3320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-10-04 |
| Decision Date | 1994-07-20 |