The following data is part of a premarket notification filed by Stryker Endoscopy with the FDA for Stryker Strykeflow Suction Irrigator Gravity Flow.
Device ID | K963646 |
510k Number | K963646 |
Device Name: | STRYKER STRYKEFLOW SUCTION IRRIGATOR GRAVITY FLOW |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | Stryker Endoscopy 2590 WALSH AVE. Santa Clara, CA 95051 -4085 |
Contact | Anthony Lee |
Correspondent | Anthony Lee Stryker Endoscopy 2590 WALSH AVE. Santa Clara, CA 95051 -4085 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-09-12 |
Decision Date | 1997-04-16 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
37613327061469 | K963646 | 000 |
37613327061353 | K963646 | 000 |
07613327051841 | K963646 | 000 |