The following data is part of a premarket notification filed by Unicor, Inc. with the FDA for Unicor, Inc. Adult Anesthesia Breathing Circuit.
| Device ID | K953787 |
| 510k Number | K953787 |
| Device Name: | UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUIT |
| Classification | Circuit, Breathing (w Connector, Adaptor, Y Piece) |
| Applicant | UNICOR, INC. 1300 25TH ST. SUITE 11 Cleveland, TN 37311 |
| Contact | Loretta J Hart |
| Correspondent | Loretta J Hart UNICOR, INC. 1300 25TH ST. SUITE 11 Cleveland, TN 37311 |
| Product Code | CAI |
| CFR Regulation Number | 868.5240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-08-14 |
| Decision Date | 1995-09-19 |