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

CONDENSATE COLLECTION KIT

K Number: K954480 · Decision Dec 29, 1995
Classifications
1
FEI Numbers
199
Registration Numbers
199
Same Product Code
183
Applicant Total
12
Review Days
94

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Basic Information

Device Name
CONDENSATE COLLECTION KIT
K Number
K954480
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5240
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nova-Ventrx
Date Received
September 26, 1995
Decision Date
December 29, 1995
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.

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Other Clearances by Nova-Ventrx

K Number Device Name
K952267 CRITERION, CRITERION I.V., MODIFIED
K893760 CRITERION I.V. VENTILATOR BREATHING CIRCUIT #1004
K881207 RES-Q 1, 2, 3, 4 AND 5
K870382 DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011
K863756 MODIFIED CRITERION VENTILATOR BREATHING CIRCUIT
K850600 CO-AX VENTILATOR CIRCUIT
K842794 MAXI-MISER HUMIDIFIER INSERT 1020 & 1021
K842795 MAXI-MISER HUMIDIFIER INSERT 1030
K841571 MAXI-MISER WATER TRANSFER SET 1021/1022
K841569 MAXI-MISER HUMIDIFIER INSERT 1020
Search all 12 clearances from Nova-Ventrx →