FLEXISTAND MAJOR
FDA 510(k) clearance K852152 · decided 1985-11-05
Clearance details
- K-number
- K852152
- Device name
- FLEXISTAND MAJOR
- Applicant
- Zygotek Assoc.
- Decision
- Substantially Equivalent
- Date received
- 1985-05-17
- Decision date
- 1985-11-05
- Days to decision
- 172 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- London W12 8nz, GB
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.