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

DEVILBISS MODEL 8500D AND 8500D-608

K Number: K894244 · Decision Oct 6, 1989
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
61
Applicant Total
29
Review Days
107

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Basic Information

Device Name
DEVILBISS MODEL 8500D AND 8500D-608
K Number
K894244
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5640
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Devilbiss Health Care, Inc.
Date Received
June 21, 1989
Decision Date
October 6, 1989
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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Other Clearances by Devilbiss Health Care, Inc.

K Number Device Name
K963349 DEVILBISS 8650D
K970289 COMPRESSOR/NEBULIZER #3650
K961126 PULSE DOSE SERIES
K950849 MODEL #7354
K952491 MODEL 7355
K952249 JET NEBULIZER
K953815 5 LPM OXYGEN CONCENTRATOR
K952037 3 LPM OXYGEN CONCENTRATOR
K946095 DEVILBISS MODEL 5500
K944611 MODEL# 7500 SURVEYOR
Search all 29 clearances from Devilbiss Health Care, Inc. →