THIGH HOLDER
FDA 510(k) clearance K832000 · decided 1983-07-12
Clearance details
- K-number
- K832000
- Device name
- THIGH HOLDER
- Applicant
- Richards Manufacturer Co.
- Decision
- Substantially Equivalent
- Date received
- 1983-06-21
- Decision date
- 1983-07-12
- Days to decision
- 21 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.