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

DISPOSABLE ANESTHESIA BREATHING CIRCUIT, MODIFIED

K Number: K922479 · Decision Oct 30, 1992
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
87
Applicant Total
29
Review Days
157

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Basic Information

Device Name
DISPOSABLE ANESTHESIA BREATHING CIRCUIT, MODIFIED
K Number
K922479
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5975
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Intertech Resources, Inc.
Date Received
May 26, 1992
Decision Date
October 30, 1992
Product Code
BZO
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
BZO Set, Tubing And Support, Ventilator (W Harness)

Similar 510(k) Clearances

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Other Clearances by Intertech Resources, Inc.

K Number Device Name
K961318 1ST RESPONSE DISPOSABLE MANOMETER
K955008 HEAT & MOISTURE EXCHANGER
K953580 HEAT MOISTURE EXCHANGER
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
K921624 DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS
Search all 29 clearances from Intertech Resources, Inc. →