The following data is part of a premarket notification filed by Quinton, Inc. with the FDA for Peritoneal Catheters With An Added Function.
| Device ID | K890288 |
| 510k Number | K890288 |
| Device Name: | PERITONEAL CATHETERS WITH AN ADDED FUNCTION |
| Classification | Catheter, Peritoneal, Long-term Indwelling |
| Applicant | QUINTON, INC. 2121 TERRY AVE. Seatle, WA 98121 |
| Contact | Ron R Duck |
| Correspondent | Ron R Duck QUINTON, INC. 2121 TERRY AVE. Seatle, WA 98121 |
| Product Code | FJS |
| CFR Regulation Number | 876.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-19 |
| Decision Date | 1989-03-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884521004115 | K890288 | 000 |
| 20884521184418 | K890288 | 000 |
| 10884521084490 | K890288 | 000 |
| 20884521084480 | K890288 | 000 |
| 20884521084473 | K890288 | 000 |
| 20884521056517 | K890288 | 000 |
| 20884521055831 | K890288 | 000 |
| 20884521084534 | K890288 | 000 |
| 10884521084513 | K890288 | 000 |
| 20884521055824 | K890288 | 000 |
| 20884521055510 | K890288 | 000 |
| 20884521055855 | K890288 | 000 |
| 10884521056770 | K890288 | 000 |
| 20884521055817 | K890288 | 000 |
| 20884521055848 | K890288 | 000 |
| 10884521086821 | K890288 | 000 |
| 10884521056732 | K890288 | 000 |
| 10884521053366 | K890288 | 000 |
| 10884521004146 | K890288 | 000 |
| 10884521004139 | K890288 | 000 |
| 10884521004122 | K890288 | 000 |
| 10884521004108 | K890288 | 000 |
| 10884521004191 | K890288 | 000 |
| 20884521084541 | K890288 | 000 |