The following data is part of a premarket notification filed by B&b Medical Assoc., Inc. with the FDA for Vac-g (guillotine Vitrector).
Device ID | K881519 |
510k Number | K881519 |
Device Name: | VAC-G (GUILLOTINE VITRECTOR) |
Classification | Instrument, Vitreous Aspiration And Cutting, Ac-powered |
Applicant | B&B MEDICAL ASSOC., INC. 4 CANAL ST. Danvers, MA 01923 |
Contact | Alden C Bertrand |
Correspondent | Alden C Bertrand B&B MEDICAL ASSOC., INC. 4 CANAL ST. Danvers, MA 01923 |
Product Code | HQE |
CFR Regulation Number | 886.4150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-04-11 |
Decision Date | 1988-09-08 |