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

PULMO-AIDE MODEL 5610D

K Number: K854520 · Decision Dec 9, 1985
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
61
Applicant Total
12
Review Days
27

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Basic Information

Device Name
PULMO-AIDE MODEL 5610D
K Number
K854520
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5640
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
The Devilbiss Co.
Date Received
November 12, 1985
Decision Date
December 9, 1985
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 The Devilbiss Co.

K Number Device Name
K874041 DEVILBISS MODEL 8500D
K872094 VACU-AIDE
K872826 ULTRA-NEB 99 ULTRASONIC NEBULIZER
K872470 DEVO/MC44 OXYGEN CONCENTRATOR
K852209 DEVO/MC29 OXYGEN CONCENTRATOR MC29D
K851695 ULTRA-NEB 100 ULTRASONIC NEBULIZER
K830174 DE VO/44 OXYGEN CONCENTRATOR #444
K801526 SURVEYOR I, RESPIRATORY COMPUTER SYSTEM
K792385 DEVO OXYGEN CONCENTRATOR, MODEL 955
K781073 PULMO-SONIC
Search all 12 clearances from The Devilbiss Co. →