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

LUMINEB I

K Number: K884722 · Decision Feb 3, 1989
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
73
Applicant Total
13
Review Days
85

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Basic Information

Device Name
LUMINEB I
K Number
K884722
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.6250
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Lumiscope Co., Inc.
Date Received
November 10, 1988
Decision Date
February 3, 1989
Product Code
BTI
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
BTI Compressor, Air, Portable

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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
K901096 LUMISCOPE ALTERNATING PRESSURE PAD & PUMP
K901726 LUMISCOPE MICRO 100
K901809 LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25
Search all 13 clearances from Lumiscope Co., Inc. →