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

MISTY OX LAMINAR DIFFUSER HUMIDIFIER

K Number: K923754 · Decision Dec 7, 1992
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
220
Applicant Total
2
Review Days
132

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Basic Information

Device Name
MISTY OX LAMINAR DIFFUSER HUMIDIFIER
K Number
K923754
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5450
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medical Molding Corp. of America
Date Received
July 28, 1992
Decision Date
December 7, 1992
Product Code
BTT
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
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

Similar 510(k) Clearances

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

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Other Clearances by Medical Molding Corp. of America

K Number Device Name
K841469 MISTY OX DISPOS. NEBULIZER