FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OPERATING TABLE ACCESSORY CLAMP

K Number: K810282 · Decision Feb 26, 1981
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
3
Applicant Total
5
Review Days
24

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Basic Information

Device Name
OPERATING TABLE ACCESSORY CLAMP
K Number
K810282
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.3750
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Minnesota Scientific, Inc.
Date Received
February 2, 1981
Decision Date
February 26, 1981
Product Code
GBJ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GBJ Prosthesis, Adhesive, External

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GBJ), ordered by most recent decision date.

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Other Clearances by Minnesota Scientific, Inc.

K Number Device Name
K872919 OMNI-TRACT CORRAL RETRACTOR
K853948 MINNESOTA SCIENTIFIC, INC. OMNI-BEAM
K853947 OMNI-TRACT CHEST WALL & LUNA RETRACTOR
K842762 OMNI-TRACT SURGICAL RETRACTOR SYS