The following data is part of a premarket notification filed by Quinton, Inc. with the FDA for Modified Perm-cath.
| Device ID | K900835 |
| 510k Number | K900835 |
| Device Name: | MODIFIED PERM-CATH |
| Classification | Catheter, Subclavian |
| Applicant | QUINTON, INC. 3303 MONTE VILLA PKWY. Bothell, WA 98021 -8906 |
| Contact | Randy Walls |
| Correspondent | Randy Walls QUINTON, INC. 3303 MONTE VILLA PKWY. Bothell, WA 98021 -8906 |
| Product Code | LFJ |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-02-22 |
| Decision Date | 1990-05-09 |