SKED STRETCHER— 510(k) K896177
Substantially EquivalentSkedco, Inc.
FDA 510(k) clearance K896177 for SKED STRETCHER, Substantially Equivalent on 1990-01-11. Applicant: Skedco, Inc..
Clearance details
- Applicant
- Skedco, Inc.
- Product code
- Code FPP
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Portland, OR, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.