Atlas FDA

VICE OR BENCH VICE

FDA 510(k) clearance K872385 · decided 1987-07-16

Clearance details

K-number
K872385
Device name
VICE OR BENCH VICE
Applicant
Med-Tool, Inc.
Decision
Substantially Equivalent
Date received
1987-06-19
Decision date
1987-07-16
Days to decision
27 days
Clearance type
Traditional
Product code
LSA
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
St. Louis, MO, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.