FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

TRANSCUTANEOUS ELECTR. NERVE STIMUL MYOSTIM 804

K Number: K853718 · Decision Dec 4, 1985
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
8
Review Days
90

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Basic Information

Device Name
TRANSCUTANEOUS ELECTR. NERVE STIMUL MYOSTIM 804
K Number
K853718
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Electro Therapeutic Devices, Inc.
Date Received
September 5, 1985
Decision Date
December 4, 1985
Product Code
GZJ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

Similar 510(k) Clearances

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

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Other Clearances by Electro Therapeutic Devices, Inc.

K Number Device Name
K981272 ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES
K875317 ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID
K863568 'MYOSTIM EX'
K863567 'TENSAID'
K853719 TRANSCUTANEOUS ELECT. NERVE STIMUL-MYOSTIM 410
K843119 ETI TENS BELT
K770686 THERATHERM