NASAL SPLINT— 510(k) K945555
Substantially EquivalentUltracell Medical Technologies, Inc.
FDA 510(k) clearance K945555 for NASAL SPLINT, Substantially Equivalent on 1995-01-19. Applicant: Ultracell Medical Technologies, Inc.. Device class: 1.
Clearance details
- Applicant
- Ultracell Medical Technologies, Inc.
- Product code
- Code LYA
- Device class
- Class 1
- Regulation
- 21 CFR 874.4780
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Old Mystic, CT, US
Recent devices under product code LYA
view allMore clearances from Ultracell Medical Technologies, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.