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

COAXIAL CIRCUITS

K Number: K932196 · Decision Jul 2, 1993
Classifications
1
FEI Numbers
199
Registration Numbers
199
Same Product Code
183
Applicant Total
17
Review Days
57

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
COAXIAL CIRCUITS
K Number
K932196
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5240
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Life Shield Healthcare Products, Inc.
Date Received
May 6, 1993
Decision Date
July 2, 1993
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)

Similar 510(k) Clearances

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

View all

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. →