POSEY BED
FDA 510(k) clearance K113357 · decided 2012-03-21
Clearance details
- K-number
- K113357
- Device name
- POSEY BED
- Applicant
- J. T. Posey Co.
- Decision
- Substantially Equivalent
- Date received
- 2011-11-14
- Decision date
- 2012-03-21
- Days to decision
- 128 days
- Clearance type
- Traditional
- Product code
- OYS
- Device class
- 1
- Regulation number
- 880.6760
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Arcadia, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| POSEY BED (K113355) | J. T. Posey Co. | 2012-05-02 |
| POSEY BED (K103817) | J. T. Posey Co. | 2011-04-22 |
Recalls involving this device
No recalls on record reference this clearance.