Atlas FDA

LTRASONIC SCANNER U.S. ALOKA SSD-500

FDA 510(k) clearance K827177 · decided 1982-04-25

Clearance details

K-number
K827177
Device name
LTRASONIC SCANNER U.S. ALOKA SSD-500
Applicant
Aloka Co., Ltd.
Decision
Substantially Equivalent
Date received
1982-02-19
Decision date
1982-04-25
Days to decision
65 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.