The following data is part of a premarket notification filed by Stryker Endoscopy with the FDA for Stryker Endoscopic Instruments And Accessories.
| Device ID | K935237 |
| 510k Number | K935237 |
| Device Name: | STRYKER ENDOSCOPIC INSTRUMENTS AND ACCESSORIES |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | Stryker Endoscopy 210 BAYPOINTE PKWY. San Jose, CA 95134 |
| Contact | Thomas Kelly |
| Correspondent | Thomas Kelly Stryker Endoscopy 210 BAYPOINTE PKWY. San Jose, CA 95134 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-11-01 |
| Decision Date | 1994-03-21 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07613327060539 | K935237 | 000 |
| 07613327052299 | K935237 | 000 |
| 07613327052282 | K935237 | 000 |
| 07613327052121 | K935237 | 000 |
| 07613327051704 | K935237 | 000 |
| 07613327051698 | K935237 | 000 |
| 07613327051681 | K935237 | 000 |
| 07613327051513 | K935237 | 000 |
| 07613327051506 | K935237 | 000 |
| 07613327051490 | K935237 | 000 |
| 07613327051483 | K935237 | 000 |
| 07613327051452 | K935237 | 000 |
| 07613327051438 | K935237 | 000 |
| 07613327051421 | K935237 | 000 |
| 07613327051414 | K935237 | 000 |
| 07613327052305 | K935237 | 000 |
| 07613327052312 | K935237 | 000 |
| 07613327057805 | K935237 | 000 |
| 07613327056297 | K935237 | 000 |
| 07613327056273 | K935237 | 000 |
| 07613327052428 | K935237 | 000 |
| 07613327052411 | K935237 | 000 |
| 07613327052404 | K935237 | 000 |
| 07613327052398 | K935237 | 000 |
| 07613327052381 | K935237 | 000 |
| 07613327052374 | K935237 | 000 |
| 07613327052367 | K935237 | 000 |
| 07613327052350 | K935237 | 000 |
| 07613327052343 | K935237 | 000 |
| 07613327052336 | K935237 | 000 |
| 07613327052329 | K935237 | 000 |
| 07613327051407 | K935237 | 000 |