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

ELECTRO-NERVE STIMULATOR TENS MODEL BIOMED 2000/A

K Number: K905570 · Decision Jun 4, 1991
Classifications
1
FEI Numbers
179
Registration Numbers
179
Same Product Code
601
Applicant Total
34
Review Days
174

Basic Information

Device Name
ELECTRO-NERVE STIMULATOR TENS MODEL BIOMED 2000/A
K Number
K905570
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
BIOMEDICAL LIFE SYSTEMS, INC.
Date Received
December 12, 1990
Decision Date
June 4, 1991
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

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Other Clearances by BIOMEDICAL LIFE SYSTEMS, INC.

K Number Device Name
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
K031427 ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS03-1
Search all 34 clearances from BIOMEDICAL LIFE SYSTEMS, INC. →