CUTINOVA CAVITY— 510(k) K952526
Substantially Equivalent for Some IndicationsBeiersdorf, Inc.
FDA 510(k) clearance K952526 for CUTINOVA CAVITY, Substantially Equivalent for Some Indications on 1995-08-14. Applicant: Beiersdorf, Inc.. Device class: 1.
Clearance details
- Applicant
- Beiersdorf, Inc.
- Product code
- Code KMF
- Device class
- Class 1
- Regulation
- 21 CFR 880.5090
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Norwalk, CT, US
Recent devices under product code KMF
view allMore clearances from Beiersdorf, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.