K240178
- 510(k) number
- K240178
- Device name
- RFG-01
- Applicant
- Zimmer Medizinsysteme GmbH DE
- Product code
- PBX — Massager, Vacuum, Radio Frequency Induced Heat
- Decision date
- 2024-07-15
- Date received
- 2024-01-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K240178.pdf
Official FDA record: K240178
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.