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

MODEL EM-IR

K Number: K810528 · Decision Mar 31, 1981
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
18
Applicant Total
8
Review Days
33

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Basic Information

Device Name
MODEL EM-IR
K Number
K810528
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1375
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Myo-Tronics Research, Inc.
Date Received
February 26, 1981
Decision Date
March 31, 1981
Product Code
KZM
Advisory Committee
Physical Medicine
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
KZM Device, Muscle Monitoring

Similar 510(k) Clearances

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

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Other Clearances by Myo-Tronics Research, Inc.

K Number Device Name
K842223 J4 MYO-MONITOR
K842224 BNS 40
K833132 MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY
K831364 TESTCORP RA
K830034 MODEL EM-2 BIOELECTRIC PROCESSOR
K813533 ELECTRIC MUSCLE STIMULATOR
K770252 MONITOR, MYO, MODEL J3