Atlas FDA

YOSHIDA-PANOURA 10

FDA 510(k) clearance K811210 · decided 1981-08-24

Clearance details

K-number
K811210
Device name
YOSHIDA-PANOURA 10
Applicant
Kaycor Intl., Ltd.
Decision
Substantially Equivalent
Date received
1981-05-04
Decision date
1981-08-24
Days to decision
112 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.