RITE-BITE BIOPSY FORCEPS
FDA 510(k) clearance K951051 · decided 1995-03-24
Clearance details
- K-number
- K951051
- Device name
- RITE-BITE BIOPSY FORCEPS
- Applicant
- Mill-Rose Laboratory
- Decision
- Substantially Equivalent
- Date received
- 1995-03-06
- Decision date
- 1995-03-24
- Days to decision
- 18 days
- Clearance type
- Traditional
- Product code
- EOQ
- Device class
- 2
- Regulation number
- 874.4680
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Mentor, OH, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.