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

OHIO RADIANT WARMER

K Number: K802365 · Decision Oct 23, 1980
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
91
Applicant Total
47
Review Days
24

Basic Information

Device Name
OHIO RADIANT WARMER
K Number
K802365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5130
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
OHIO MEDICAL PRODUCTS
Date Received
September 29, 1980
Decision Date
October 23, 1980
Product Code
FMT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FMT Warmer, Infant Radiant

Similar 510(k) Clearances

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Other Clearances by OHIO MEDICAL PRODUCTS

K Number Device Name
K841733 OHIO WASTE GAS SCAVENGING RESERVOIR
K842003 OHIO WASTE GAS SCAVENGING INTERFACE
K840356 OHIO UNITROL II ANESTHESIA GAS MACHINE
K841274 BAG-TO-VENTILATOR SELECTOR VALVE
K840857 OHIO 3000 INFANT WARMER SYSTEM
K840858 OHIO 3300 INFANT WARMER SYSTEM
K840967 OHIO HEAT REFLECTING PATCH
K840453 MEDISHIELD PVM RESPIROMETER
K840452 PREMIUM DABM DISPOS. ANES. BREATH MASK
K833335 MODULUS II ANESTHESIA GAS MACHINE
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