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

LUMISCOPE ALTERNATING PRESSURE PAD & PUMP

K Number: K901096 · Decision Aug 21, 1990
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
101
Applicant Total
13
Review Days
167

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Basic Information

Device Name
LUMISCOPE ALTERNATING PRESSURE PAD & PUMP
K Number
K901096
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5550
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Lumiscope Co., Inc.
Date Received
March 7, 1990
Decision Date
August 21, 1990
Product Code
FNM
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
FNM Mattress, Air Flotation, Alternating Pressure

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Other Clearances by Lumiscope Co., Inc.

K Number Device Name
K032714 CARDICARE MODEL MT-301F & MT-301C
K954792 LUMISCOPE MODEL 2018 THERMOMETER
K931768 INTERFERENTIAL CURRENT THERAPY UNIT
K925054 INFRARED LAMP
K924081 LUMISONIC
K920099 GYMMAN
K901849 LUMISCOPE EMS 8000
K901726 LUMISCOPE MICRO 100
K901809 LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25
K894127 LUMISCOPE MODEL 1000/APCC MODEL 1000
Search all 13 clearances from Lumiscope Co., Inc. →