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 |