The following data is part of a premarket notification filed by Medical Instrument Development Laboratories, Inc. with the FDA for Vit Enhancer.
| Device ID | K992943 |
| 510k Number | K992943 |
| Device Name: | VIT ENHANCER |
| Classification | Instrument, Vitreous Aspiration And Cutting, Ac-powered |
| Applicant | MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC. 14477 CATALINA ST. San Leandro, CA 94577 |
| Contact | Linda M Upton |
| Correspondent | Linda M Upton MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC. 14477 CATALINA ST. San Leandro, CA 94577 |
| Product Code | HQE |
| CFR Regulation Number | 886.4150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-31 |
| Decision Date | 1999-12-10 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VIT ENHANCER 77036135 3390699 Dead/Cancelled |
Medical Instrument Development Laboratories, Inc. 2006-11-03 |
![]() VIT ENHANCER 75850033 not registered Dead/Abandoned |
Medical Instrument Development Labs, Inc 1999-12-02 |