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

EVOLUTION ULTRASONIC

K Number: K894215 · Decision Apr 16, 1990
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
61
Applicant Total
19
Review Days
301

Basic Information

Device Name
EVOLUTION ULTRASONIC
K Number
K894215
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5640
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
MEDICAL INDUSTRIES AMERICA, INC.
Date Received
June 19, 1989
Decision Date
April 16, 1990
Product Code
CCQ
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
CCQ Nebulizer, Medicinal, Non-Ventilatory (Atomizer)

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K002763 REMREST
K011053 OPTIMA
K964078 3050 SPORT-NEB
K943990 3000 AEROSOL TWO
K942444 3002 AEROMAX
K941961 605 VACU-MAX
K942208 4003 AEROLITE
K940630 503 MAXI COMPRESSOR
Search all 19 clearances from MEDICAL INDUSTRIES AMERICA, INC. →