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

97-D EMERSON DIMMER CONTROL

K Number: K872936 · Decision Sep 24, 1987
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
23
Applicant Total
25
Review Days
59

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Basic Information

Device Name
97-D EMERSON DIMMER CONTROL
K Number
K872936
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3725
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
J. H. Emerson Co.
Date Received
July 27, 1987
Decision Date
September 24, 1987
Product Code
IQA
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IQA System, Environmental Control, Powered

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Other Clearances by J. H. Emerson Co.

K Number Device Name
K002598 EMERSON COUGH ASSIST MODEL CA-3000 W/AUTOMATIC TIMING AND MODEL CM-3000 W/MANUAL TIMING
K920910 OXYGEN POWERED RESUSCITATOR FOR CPR
K924174 EMERSON IN-EXSUFFLATOR, MODELS 2-CM & 2-CA
K902764 EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM
K896721 MODEL 7-AT TREATMENT CHAMBER
K881808 EMERSON CHEST RESPIRATOR, MODEL 33-CRE
K873489 EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000
K872937 97-TD EMERSON TIMER/DIMMER CONTROL
K864379 EMERSON 3MV VOLUME VENTILATOR
K864394 EMERSON 3MV VOLUME VENTILATOR
Search all 25 clearances from J. H. Emerson Co. →