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

BIOEMG III

K Number: K082927 · Decision Feb 6, 2009
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
18
Applicant Total
10
Review Days
128

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Basic Information

Device Name
BIOEMG III
K Number
K082927
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1375
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Research Associates, Inc.
Date Received
October 1, 2008
Decision Date
February 6, 2009
Product Code
KZM
Advisory Committee
Physical Medicine
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
KZM Device, Muscle Monitoring

Similar 510(k) Clearances

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

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Other Clearances by Bio-Research Associates, Inc.

K Number Device Name
K130158 M-SCAN
K061799 QUADRATENS, MODEL QT-42
K003176 BIOEMG II AND BIOJVA
K991756 3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE
K981563 BIOPAK MEASUREMENT SYSTEM
K952218 JT-3 ELECTROGNATHOGRAPH
K873947 BIO-EMG MODEL 800
K844618 BIO-TENS
K822565 NEEDLE CATHETER JEJUNOSTOMY KIT