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

GENESIS INSUFFLATING CATHETER

K Number: K903669 · Decision Sep 12, 1990
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
15
Review Days
30

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Basic Information

Device Name
GENESIS INSUFFLATING CATHETER
K Number
K903669
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
General Medical Co.
Date Received
August 13, 1990
Decision Date
September 12, 1990
Product Code
BSY
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSY Catheters, Suction, Tracheobronchial

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K Number Device Name
K926269 PROCEDURE KIT
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K900110 OPERAND* LUBRICATING JELLY
K853635 SUBDERM TM
K844652 C.A.S.E. CONTAINER
K831320 DRIONIC
K820689 C.S.R. WRAPPERS
K820521 STERILIZATION WRAP
K802231 AIR VIVA II
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