The following data is part of a premarket notification filed by Unicor, Inc. with the FDA for Unicor, Inc. Corrugated Tubing.
| Device ID | K953784 |
| 510k Number | K953784 |
| Device Name: | UNICOR, INC. CORRUGATED TUBING |
| Classification | Set, Tubing And Support, Ventilator (w Harness) |
| Applicant | UNICOR, INC. 151 GOLD STAR DR., S.W. Cleveland, TN 37323 |
| Contact | Loretta J Hart |
| Correspondent | Loretta J Hart UNICOR, INC. 151 GOLD STAR DR., S.W. Cleveland, TN 37323 |
| Product Code | BZO |
| CFR Regulation Number | 868.5975 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-08-14 |
| Decision Date | 1995-09-19 |