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

LIFE SHIELD HEALTHCARE PRODUCTS BREATHING FILTER

K Number: K925388 · Decision May 11, 1993
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
17
Review Days
197

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Basic Information

Device Name
LIFE SHIELD HEALTHCARE PRODUCTS BREATHING FILTER
K Number
K925388
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Life Shield Healthcare Products, Inc.
Date Received
October 26, 1992
Decision Date
May 11, 1993
Product Code
CAH
Advisory Committee
Anesthesiology
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
CAH Filter, Bacterial, Breathing-Circuit

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CAH), ordered by most recent decision date.

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Other Clearances by Life Shield Healthcare Products, Inc.

K Number Device Name
K932562 GAS SAMPLING LINES AND CONNECTORS
K932561 GUEDEL AIRWAYS
K932557 HYPERINFLATION SYSTEM
K932560 VOLUME VENTILATORS
K932558 ADULT ANESTHESIA BREATHING CIRCUIT
K932559 MAPLESON D CIRCUITS
K932563 VENTILATOR HOSES
K932191 BREATHING BAGS
K932193 PEDIATRIC TEMPERATURE MONITORING CIRCUITS
K932195 ADULT GAS SAMPLING CIRCUITS
Search all 17 clearances from Life Shield Healthcare Products, Inc. →