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

AQUA-SEAL

K Number: K761202 · Decision Dec 9, 1976
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
47
Applicant Total
26
Review Days
2

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Basic Information

Device Name
AQUA-SEAL
K Number
K761202
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Respiratory Care, Inc.
Date Received
December 7, 1976
Decision Date
December 9, 1976
Product Code
KDQ
Advisory Committee
General Hospital
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
KDQ Bottle, Collection, Vacuum

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
K864147 AQUAVALVE
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
Search all 26 clearances from Respiratory Care, Inc. →