BONE MILL BONE GRINDER
FDA 510(k) clearance K842845 · decided 1984-10-25
Clearance details
- K-number
- K842845
- Device name
- BONE MILL BONE GRINDER
- Applicant
- Acromed Corp.
- Decision
- Substantially Equivalent
- Date received
- 1984-07-20
- Decision date
- 1984-10-25
- Days to decision
- 97 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Cleveland, OH, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.