Atlas FDA

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.