Atlas FDA

YOSHIDA/KAYCOR X-70 X-RAY UNIT

FDA 510(k) clearance K828325 · decided 1982-10-21

Clearance details

K-number
K828325
Device name
YOSHIDA/KAYCOR X-70 X-RAY UNIT
Applicant
The Yoshida Dental Mfg. Co., Ltd.
Decision
Substantially Equivalent
Date received
1982-09-28
Decision date
1982-10-21
Days to decision
23 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.