The following data is part of a premarket notification filed by Ultracell Medical Technologies, Inc. with the FDA for Nasal Splint.
| Device ID | K945555 |
| 510k Number | K945555 |
| Device Name: | NASAL SPLINT |
| Classification | Splint, Intranasal Septal |
| Applicant | ULTRACELL MEDICAL TECHNOLOGIES, INC. POST OFFICE BOX 609 Old Mystic, CT 06372 |
| Contact | George P Korteweg |
| Correspondent | George P Korteweg ULTRACELL MEDICAL TECHNOLOGIES, INC. POST OFFICE BOX 609 Old Mystic, CT 06372 |
| Product Code | LYA |
| CFR Regulation Number | 874.4780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-11-14 |
| Decision Date | 1995-01-19 |