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

PMP, LTD. PEDIATRIC TEMPERATURE MONITORING CIRCUIT

K Number: K932486 · Decision Jul 21, 1993
Classifications
1
FEI Numbers
199
Registration Numbers
199
Same Product Code
183
Applicant Total
16
Review Days
58

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Basic Information

Device Name
PMP, LTD. PEDIATRIC TEMPERATURE MONITORING CIRCUIT
K Number
K932486
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5240
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Precision Med Products, Ltd.
Date Received
May 24, 1993
Decision Date
July 21, 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)

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Other Clearances by Precision Med Products, Ltd.

K Number Device Name
K932710 GAS SAMPLING LINES AND CONNECTORS
K932711 PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS
K932707 ADULT ANESTHESIA BREATHING CIRCUIT
K932706 PRECISION MED PRODUCTS LTD. VENTILATOR HOSE
K932709 PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM
K932708 PRECISION MED PRODUCTS LTD MAPLESON D CIRCUITS
K932488 PMP, LTD. PEDIATRIC GAS SAMPLING CIRCUITS
K932489 PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR.
K932712 PRECISION MED PRODUCTS LTD VOLUME VENTILATORS
K932497 PRECISION MED PRODUCTS, LTD. ADULT GAS SAMPLING
Search all 16 clearances from Precision Med Products, Ltd. →