MODEL LS 3000 LINEAR SCANNER
FDA 510(k) clearance K827377 · decided 1982-07-13
Clearance details
- K-number
- K827377
- Device name
- MODEL LS 3000 LINEAR SCANNER
- Applicant
- Hitachi Medical Corp.
- Decision
- Substantially Equivalent
- Date received
- 1982-04-20
- Decision date
- 1982-07-13
- Days to decision
- 84 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Tokyo, JP
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.