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

DEVILBISS MODEL 6300D

K Number: K896090 · Decision Nov 30, 1989
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
1
Applicant Total
29
Review Days
42

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Basic Information

Device Name
DEVILBISS MODEL 6300D
K Number
K896090
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.5220
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Devilbiss Health Care, Inc.
Date Received
October 19, 1989
Decision Date
November 30, 1989
Product Code
EPN
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EPN Pump, Nebulizer, Manual

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EPN), ordered by most recent decision date.

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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. →