FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SKYVAL

K Number: K973610 · Decision Dec 19, 1997
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
1
Review Days
88

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Basic Information

Device Name
SKYVAL
K Number
K973610
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5070
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pyramid Air Systems
Date Received
September 22, 1997
Decision Date
December 19, 1997
Product Code
FYD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FYD Apparatus, Exhaust, Surgical

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