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

AQUAVALVE

K Number: K864147 · Decision Dec 5, 1986
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
21
Applicant Total
26
Review Days
44

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Basic Information

Device Name
AQUAVALVE
K Number
K864147
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5995
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Respiratory Care, Inc.
Date Received
October 22, 1986
Decision Date
December 5, 1986
Product Code
BYH
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
BYH Drain, Tee (Water Trap)

Similar 510(k) Clearances

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Other Clearances by Respiratory Care, Inc.

K Number Device Name
K892230 RCI VIRAL/BACTERIAL FILTER
K884150 MODIFIED CONCHATHERM III CONTROLLED HEATER
K881625 CONCHATHERM III PLUS DUAL HEAT WIRE SERVO CONTROLL
K863955 COLBY LEVEL ALARM
K861555 CIRCAPAK UNIVERSAL VOLUME VENTILATOR CIRCUIT
K834151 CONCHATHERM LHF HUMIDIFIER HEATER
K833974 AQUAPAK 020 HUMIDIFIER ADAPTER
K832453 SLIMB SINGLE LIMB BREATHING CIRCUIT
K811524 AQUACADE
K811073 A QUAPAK
Search all 26 clearances from Respiratory Care, Inc. →