The following data is part of a premarket notification filed by Micor, Inc. with the FDA for Percutaneous Catheters.
| Device ID | K860339 |
| 510k Number | K860339 |
| Device Name: | PERCUTANEOUS CATHETERS |
| Classification | Catheter, Percutaneous |
| Applicant | MICOR, INC. 9229 PANNIER RD. Pittsburgh, PA 15237 |
| Contact | Stephen Brushey |
| Correspondent | Stephen Brushey MICOR, INC. 9229 PANNIER RD. Pittsburgh, PA 15237 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-01-29 |
| Decision Date | 1986-03-31 |