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

MICROFLOW

K Number: K924684 · Decision Dec 15, 1992
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
20
Review Days
90

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Basic Information

Device Name
MICROFLOW
K Number
K924684
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mountain Medical Equipment, Inc.
Date Received
September 16, 1992
Decision Date
December 15, 1992
Product Code
CAF
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
CAF Nebulizer (Direct Patient Interface)

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Other Clearances by Mountain Medical Equipment, Inc.

K Number Device Name
K941793 OXYGEN CONCENTRATION STATUS INDICATOR (O.C.S.I.)
K923650 SCOTTY
K914916 ALPINE V
K902890 ASPEN 3 OXYGEN CONCENTRATOR
K893531 CUFF SPECULUM
K884084 PORTABLE OXYGEN GENERATOR
K881802 ALPINE PORTABLE OXYGEN GENERATOR
K873677 ECONO-MIST PORTABLE COMPRESSOR DRIVEN NEBULIZER
K873170 ARIES
K864005 ALPINE
Search all 20 clearances from Mountain Medical Equipment, Inc. →