FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

AM 706 ELECTROMYOGRAPH, STIM., NEURO., EXTERNAL

K Number: K881196 · Decision Jun 16, 1989
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
9
Review Days
452

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Basic Information

Device Name
AM 706 ELECTROMYOGRAPH, STIM., NEURO., EXTERNAL
K Number
K881196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Biometer Intl. A/S
Date Received
March 21, 1988
Decision Date
June 16, 1989
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

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K893485 ACCELOGRAPH NEUROMUSCULAR TRANSMISSION MONITOR
K890746 MYOTEST DBS NERVE STIMULATOR
K870619 ACCELOGRAPH
K860186 MYOTEST - NERVE STIMULATOR
K860187 MYOGRAPH 2000 - NEURO. TRANS. MONITOR & RECORDING