The following data is part of a premarket notification filed by Smith & Nephew Richards, Inc. with the FDA for Accessories For Endoscopes For Sinus Surgery.
Device ID | K932988 |
510k Number | K932988 |
Device Name: | ACCESSORIES FOR ENDOSCOPES FOR SINUS SURGERY |
Classification | Nasopharyngoscope (flexible Or Rigid) |
Applicant | SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. Bartlett, TN 38133 |
Contact | Jeff Cobb |
Correspondent | Jeff Cobb SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. Bartlett, TN 38133 |
Product Code | EOB |
CFR Regulation Number | 874.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-06-18 |
Decision Date | 1993-07-26 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00821925041387 | K932988 | 000 |
00821925019096 | K932988 | 000 |
00821925019089 | K932988 | 000 |
00821925019072 | K932988 | 000 |
00821925018990 | K932988 | 000 |
00821925018945 | K932988 | 000 |
00821925018280 | K932988 | 000 |
00821925018273 | K932988 | 000 |
00821925018266 | K932988 | 000 |
00821925018259 | K932988 | 000 |
00821925019126 | K932988 | 000 |
00821925019911 | K932988 | 000 |
00821925019928 | K932988 | 000 |
00821925016842 | K932988 | 000 |
00821925029910 | K932988 | 000 |
00821925029903 | K932988 | 000 |
00821925029866 | K932988 | 000 |
00821925024168 | K932988 | 000 |
00821925022973 | K932988 | 000 |
00821925022737 | K932988 | 000 |
00821925022713 | K932988 | 000 |
00821925022706 | K932988 | 000 |
00821925018044 | K932988 | 000 |