CHROMOPHARE
Device, Medical Examination, Ac Powered
BERCHTOLD HOLDING GMBH
The following data is part of a premarket notification filed by Berchtold Holding Gmbh with the FDA for Chromophare.
Pre-market Notification Details
| Device ID | K935832 |
| 510k Number | K935832 |
| Device Name: | CHROMOPHARE |
| Classification | Device, Medical Examination, Ac Powered |
| Applicant | BERCHTOLD HOLDING GMBH LUDWIGSTALER STR. 25 Tuttlingen, DE D-78532 |
| Contact | W Hill |
| Correspondent | W Hill BERCHTOLD HOLDING GMBH LUDWIGSTALER STR. 25 Tuttlingen, DE D-78532 |
| Product Code | KZF |
| CFR Regulation Number | 880.6320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-12-07 |
| Decision Date | 1994-02-03 |
Trademark Results [CHROMOPHARE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CHROMOPHARE 73351500 1292017 Live/Registered |
Gebruder Martin 1982-02-22 |
 CHROMOPHARE 73311128 1205348 Live/Registered |
Elmed Incorporated 1981-05-19 |
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