The following data is part of a premarket notification filed by Sterilab, Inc. with the FDA for Sterilab Cannulas, Sterilab Cystotmes, Sterilab Needles And Sterilab Lens Manipulators.
| Device ID | K961524 |
| 510k Number | K961524 |
| Device Name: | STERILAB CANNULAS, STERILAB CYSTOTMES, STERILAB NEEDLES AND STERILAB LENS MANIPULATORS |
| Classification | Cystotome |
| Applicant | STERILAB, INC. 6068 CORTE DEL CEDRO Carlsbad, CA 92009 |
| Contact | Jonathan Woodward |
| Correspondent | Jonathan Woodward STERILAB, INC. 6068 CORTE DEL CEDRO Carlsbad, CA 92009 |
| Product Code | HNY |
| Subsequent Product Code | GAA |
| Subsequent Product Code | HMX |
| Subsequent Product Code | KDC |
| CFR Regulation Number | 886.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-04-22 |
| Decision Date | 1996-05-16 |