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

COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, MODEL BMLS04-1

K Number: K041388 · Decision Nov 23, 2004
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
35
Review Days
182

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Basic Information

Device Name
COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, MODEL BMLS04-1
K Number
K041388
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
May 25, 2004
Decision Date
November 23, 2004
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
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
K031427 ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS03-1
Search all 35 clearances from Biomedical Life Systems, Inc. →