PRO-LOK EXTENSION SET
FDA 510(k) clearance K933852 · decided 1993-12-29
Clearance details
- K-number
- K933852
- Device name
- PRO-LOK EXTENSION SET
- Applicant
- Beech Medical Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1993-08-06
- Decision date
- 1993-12-29
- Days to decision
- 145 days
- Clearance type
- Traditional
- Product code
- FPA
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Newtown, PA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.