BURTON H- BASE TABLE - MODEL 1990
FDA 510(k) clearance K924773 · decided 1993-06-07
Clearance details
- K-number
- K924773
- Device name
- BURTON H- BASE TABLE - MODEL 1990
- Applicant
- R.H. Burton Co.
- Decision
- Substantially Equivalent
- Date received
- 1992-09-23
- Decision date
- 1993-06-07
- Days to decision
- 257 days
- Clearance type
- Traditional
- Product code
- HRX
- Device class
- 2
- Regulation number
- 888.1100
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Grove City, OH, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.