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

PADGETT SUCTION CANNULA

K Number: K833717 · Decision Dec 14, 1983
Classifications
1
FEI Numbers
378
Registration Numbers
378
Same Product Code
35
Applicant Total
22
Review Days
54

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Basic Information

Device Name
PADGETT SUCTION CANNULA
K Number
K833717
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Advanced Biosearch Assn.
Date Received
October 21, 1983
Decision Date
December 14, 1983
Product Code
GEA
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
GEA Cannula, Surgical, General & Plastic Surgery

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