FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

TRANSTEK GLASS BODY ANALYZER; TRANSTEK GLASS BODY ANALYZER; TRANSTEK GLASS BODY ANALYZER;TRANSTEK GLASS BODY ANALYZER

K Number: K102191 · Decision May 2, 2011
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
78
Applicant Total
9
Review Days
272

Basic Information

Device Name
TRANSTEK GLASS BODY ANALYZER; TRANSTEK GLASS BODY ANALYZER; TRANSTEK GLASS BODY ANALYZER;TRANSTEK GLASS BODY ANALYZER
K Number
K102191
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.2770
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ZHONGSHAN TRANSTEK ELECTRONICS CO., LTD.
Date Received
August 3, 2010
Decision Date
May 2, 2011
Product Code
MNW
Advisory Committee
Cardiovascular
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
MNW Analyzer, Body Composition

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K Number Device Name
K123780 TRANSTEK BLOOD PRESSURE MONITOR
K123781 TRANSTEK GLASS BODY FAT ANALYZER
K123669 TRANSTEK WRIST BLOOD PRESSURE MONITOR
K122482 TRANSTEK WRIST BLOOD PRESSURE MONITOR
K121971 WITHINGS, SMART BODY SCALE
K120058 TRANSTEK BLOOD PRESSURE MONITOR
K112932 TRANSTEK
K101681 TRANSTEK BLOOD PRESSURE MONITOR MODEL TMB-986, TMB-987, TMB-995