The following data is part of a premarket notification filed by Gynex Corp. with the FDA for Gynex Endospeculum.
| Device ID | K980237 |
| 510k Number | K980237 |
| Device Name: | GYNEX ENDOSPECULUM |
| Classification | Instrument, Manual, Specialized Obstetric-gynecologic |
| Applicant | GYNEX CORP. 1000 BURNETT AVE. SUITE 450 Concord, CA 94520 |
| Contact | David W Schlerf |
| Correspondent | David W Schlerf GYNEX CORP. 1000 BURNETT AVE. SUITE 450 Concord, CA 94520 |
| Product Code | KNA |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-01-23 |
| Decision Date | 1998-04-08 |
| Summary: | summary |