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

TORQUE PLUS CATALOG 30120

K Number: K833940 · Decision Dec 28, 1983
Classifications
1
FEI Numbers
387
Registration Numbers
387
Same Product Code
75
Applicant Total
83
Review Days
43

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Basic Information

Device Name
TORQUE PLUS CATALOG 30120
K Number
K833940
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Concept, Inc.
Date Received
November 15, 1983
Decision Date
December 28, 1983
Product Code
HWE
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

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