PATHFORMER
FDA 510(k) clearance K052770 · decided 2005-10-31
Clearance details
- K-number
- K052770
- Device name
- PATHFORMER
- Applicant
- Path Scientific, LLC
- Decision
- Substantially Equivalent
- Date received
- 2005-09-30
- Decision date
- 2005-10-31
- Days to decision
- 31 days
- Clearance type
- Traditional
- Product code
- NWF
- Device class
- 1
- Regulation number
- 878.4820
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Chevy Chase, MD, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.