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

THERA PULSE A ELECTRO NERVE STIMULATOR

K Number: K925686 · Decision Mar 18, 1993
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
35
Review Days
126

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Basic Information

Device Name
THERA PULSE A ELECTRO NERVE STIMULATOR
K Number
K925686
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biomedical Life Systems, Inc.
Date Received
November 12, 1992
Decision Date
March 18, 1993
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 Biomedical Life Systems, Inc.

K Number Device Name
K172971 BMLS16-1
K102051 PAIN BUDDY
K061476 ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-1
K042711 MODEL BMLS03-7
K041388 COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, MODEL BMLS04-1
K040007 INTERFERENTIAL STIMULATOR, MODEL BMLS02-6
K033174 BMLS03-3
K040824 INTERFERENTIAL STIMULATOR, MODEL BMLS03-6
K040306 HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7
K033455 ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5
Search all 35 clearances from Biomedical Life Systems, Inc. →