The following data is part of a premarket notification filed by Pb Diagnostic Systems, Inc. with the FDA for Opus(r) Lh Test System.
| Device ID | K913938 |
| 510k Number | K913938 |
| Device Name: | OPUS(R) LH TEST SYSTEM |
| Classification | Radioimmunoassay, Luteinizing Hormone |
| Applicant | PB DIAGNOSTIC SYSTEMS, INC. 151 UNIVERSITY AVE. Westwood, MA 02090 |
| Contact | Lori Baranauskas |
| Correspondent | Lori Baranauskas PB DIAGNOSTIC SYSTEMS, INC. 151 UNIVERSITY AVE. Westwood, MA 02090 |
| Product Code | CEP |
| CFR Regulation Number | 862.1485 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-09-03 |
| Decision Date | 1991-11-07 |