ENDOSCOPE
Endoscope, Fiber Optic
CUDA PRODUCTS CO.
The following data is part of a premarket notification filed by Cuda Products Co. with the FDA for Endoscope.
Pre-market Notification Details
| Device ID | K935818 |
| 510k Number | K935818 |
| Device Name: | ENDOSCOPE |
| Classification | Endoscope, Fiber Optic |
| Applicant | CUDA PRODUCTS CO. 6000 POWERS AVE. Jacksonville, FL 32217 |
| Contact | Joseph Cuda |
| Correspondent | Joseph Cuda CUDA PRODUCTS CO. 6000 POWERS AVE. Jacksonville, FL 32217 |
| Product Code | GDB |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-12-02 |
| Decision Date | 1994-07-13 |
Trademark Results [ENDOSCOPE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ENDOSCOPE 98127497 not registered Live/Pending |
CHEN, XIAOFENG 2023-08-10 |
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