FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

ANAESLOCK THREE VAPORIZER INTERLOCK HVA003

K Number: K843993 · Decision Nov 15, 1984
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
56
Applicant Total
10
Review Days
35

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Basic Information

Device Name
ANAESLOCK THREE VAPORIZER INTERLOCK HVA003
K Number
K843993
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5880
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Southmedic, Inc.
Date Received
October 11, 1984
Decision Date
November 15, 1984
Product Code
CAD
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
CAD Vaporizer, Anesthesia, Non-Heated

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Other Clearances by Southmedic, Inc.

K Number Device Name
K222511 Oxy2Pro
K131410 CO2/O2 NASAL CANNULA (WITH 4 (10CM) O2 AND CO2 TUBE), CO2/O2 NASAL CANNULA (WITH 8 (240CM) O2 AND 4 (10CM) CO2 TUBE),
K101953 SMDIA-1000
K014211 OXYARM CO2
K945993 VAPOFIL
K923265 FUNNEL ADAPTOR
K863318 AEROSOL-T
K861839 VAPOFIL
K860545 VAPORIZER SPACER