The following data is part of a premarket notification filed by Accurate Surgical Instruments Co. with the FDA for Trocar (faller Stylet).
Device ID | K910786 |
510k Number | K910786 |
Device Name: | TROCAR (FALLER STYLET) |
Classification | Catheter, Peritoneal, Long-term Indwelling |
Applicant | ACCURATE SURGICAL INSTRUMENTS CO. 590 RICHMOND STREET WEST Toronto Canado M5v 1y9, CA M5v 1y9 |
Contact | Helen Moreland |
Correspondent | Helen Moreland ACCURATE SURGICAL INSTRUMENTS CO. 590 RICHMOND STREET WEST Toronto Canado M5v 1y9, CA M5v 1y9 |
Product Code | FJS |
CFR Regulation Number | 876.5630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-02-25 |
Decision Date | 1991-09-19 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10884521004788 | K910786 | 000 |
10884521811263 | K910786 | 000 |