Atlas FDA

UNIMIDE

FDA 510(k) clearance K042284 · decided 2004-12-03

Clearance details

K-number
K042284
Device name
UNIMIDE
Applicant
United Medical Industries Co. , Ltd.
Decision
Substantially Equivalent
Date received
2004-08-24
Decision date
2004-12-03
Days to decision
101 days
Clearance type
Traditional
Product code
GAR
Device class
2
Regulation number
878.5020
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Riyadh, Central Province, SA
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.