The following data is part of a premarket notification filed by Coburn Optical Ind., Inc. with the FDA for Eye-vac.
Device ID | K801231 |
510k Number | K801231 |
Device Name: | EYE-VAC |
Classification | Instrument, Vitreous Aspiration And Cutting, Battery-powered |
Applicant | COBURN OPTICAL IND., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | HKP |
CFR Regulation Number | 886.4150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-05-27 |
Decision Date | 1980-07-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EYE-VAC 78267368 3181491 Live/Registered |
JPAULJONES, L.P. 2003-06-26 |
EYE-VAC 73289676 1397537 Dead/Cancelled |
Coburn Optical Industries, Inc. 1980-12-15 |