FOGLESS
Anti Fog Solution And Accessories, Endoscopy
SOREX MEDICAL
The following data is part of a premarket notification filed by Sorex Medical with the FDA for Fogless.
Pre-market Notification Details
| Device ID | K923843 |
| 510k Number | K923843 |
| Device Name: | FOGLESS |
| Classification | Anti Fog Solution And Accessories, Endoscopy |
| Applicant | SOREX MEDICAL 5725 WEST HAROLD GATTY DR. Salt Lake City, UT 84116 |
| Contact | Douglas Jacob |
| Correspondent | Douglas Jacob SOREX MEDICAL 5725 WEST HAROLD GATTY DR. Salt Lake City, UT 84116 |
| Product Code | OCT |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-07-31 |
| Decision Date | 1994-03-25 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884521066557 | K923843 | 000 |
| 10884521066540 | K923843 | 000 |
Trademark Results [FOGLESS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FOGLESS 78267031 not registered Dead/Abandoned |
Conair Corporation 2003-06-25 |
 FOGLESS 73237454 1160755 Live/Registered |
H. L. Bouton Company, Inc. 1979-10-31 |
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