X-RAY BEAM FILTER
FDA 510(k) clearance K837334 · decided 1983-04-22
Clearance details
- K-number
- K837334
- Device name
- X-RAY BEAM FILTER
- Applicant
- Eastman Kodak Company
- Decision
- Substantially Equivalent
- Date received
- 1983-03-30
- Decision date
- 1983-04-22
- Days to decision
- 23 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Rochester, NY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.