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

SURGAIRTOME TWO

K Number: K781979 · Decision Dec 20, 1978
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
55
Applicant Total
36
Review Days
23

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Basic Information

Device Name
SURGAIRTOME TWO
K Number
K781979
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
American Sterilizer Co.
Date Received
November 27, 1978
Decision Date
December 20, 1978
Product Code
HSZ
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
HSZ Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment

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K922485 CHEMDI-VHP CHEMICAL INDICATOR
K930493 QUANTUM 3080 SURGICAL TABLE
K905816 ORTHOVISION TABLE
K896674 AMSCO QUANTUM LIGHT
K895164 EAGLE DS
K882660 GENERAL SURGICAL TABLE AND ACCESSORIES
K880198 GEMINI SURGICAL LIGHT
K864846 RADIOGRAPHIC - LEG SECTION
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