ALCYON ROTATIONAL COBALT THERAPY
FDA 510(k) clearance K837465 · decided 1983-06-28
Clearance details
- K-number
- K837465
- Device name
- ALCYON ROTATIONAL COBALT THERAPY
- Applicant
- Cgr Medical Corp.
- Decision
- Substantially Equivalent
- Date received
- 1983-05-03
- Decision date
- 1983-06-28
- Days to decision
- 56 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Columbia, MD, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.