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

DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED

K Number: K912065 · Decision Oct 23, 1991
Classifications
1
FEI Numbers
199
Registration Numbers
199
Same Product Code
183
Applicant Total
29
Review Days
180

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Basic Information

Device Name
DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED
K Number
K912065
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5240
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Intertech Resources, Inc.
Date Received
April 26, 1991
Decision Date
October 23, 1991
Product Code
CAI
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
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece)

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K952223 XENON GAS BREATHING CIRCUIT
K952062 PFT FILTER
K952169 SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRIC
K952214 SIMS INTERTECH HYPERINFLATION BAG SYSTEM
K935036 HEPA FILTERED HEAT AND MOISTURE EXCHANGER
K930816 HEPA FILTERED HME
K922479 DISPOSABLE ANESTHESIA BREATHING CIRCUIT, MODIFIED
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