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

ACHILLES

K Number: K103633 · Decision May 11, 2011
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
8
Applicant Total
12
Review Days
149

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Basic Information

Device Name
ACHILLES
K Number
K103633
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1180
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Medical Systems China Co., Ltd.
Date Received
December 13, 2010
Decision Date
May 11, 2011
Product Code
MUA
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
MUA Bone Sonometer

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Other Clearances by Ge Medical Systems China Co., Ltd.

K Number Device Name
K151063 Monitor B40
K142288 MAC 800 Resting ECG Analysis System
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K130584 MONITOR B40
K122253 PROCARE MONITOR B20
K123238 ACHILLES
K120598 PROCARE MONITOR B40
K102256 GE LOGIQ I/E & VIVID E COMPACT DIAGNOSTIC ULTRASOUND
K102113 GE VENUE 40 COMPACT DIAGNOSTIC ULTRASOUND
K091374 GE LOGIQ I/E & VIVID E COMPACT ULTRASOUND
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