DESCRIBE PFD Patch— 510(k) K172689
Substantially EquivalentMerz North America, Inc.
FDA 510(k) clearance K172689 for DESCRIBE PFD Patch, Substantially Equivalent on 2017-11-29. Applicant: Merz North America, Inc.. Device class: 2.
Clearance details
- Applicant
- Merz North America, Inc.
- Product code
- Code PKO
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raleigh, NC, US
Recent devices under product code PKO
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