PRONE POSITIONER
FDA 510(k) clearance K932187 · decided 1993-06-01
Clearance details
- K-number
- K932187
- Device name
- PRONE POSITIONER
- Applicant
- Voss Medical Products
- Decision
- Substantially Equivalent
- Date received
- 1993-05-05
- Decision date
- 1993-06-01
- Days to decision
- 27 days
- Clearance type
- Traditional
- Product code
- KIL
- Device class
- 1
- Regulation number
- 888.4540
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Washington, DC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.