ACHILLES EXPRESS ULTRASONOMETER

FDA Premarket Approval P970040 S003

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Approval for a manufacturing site located at ge medical systems china co. , ltd. , jiansgu, p. R. China.

DeviceACHILLES EXPRESS ULTRASONOMETER
Generic NameBone Sonometer
ApplicantGE LUNAR CORP.
Date Received2004-07-15
Decision Date2004-07-30
PMAP970040
SupplementS003
Product CodeMUA 
Advisory CommitteeRadiology
Supplement TypeNormal 180 Day Track No User Fee
Supplement ReasonExpress Gmp Supplement
Expedited ReviewNo
Combination Product No
Applicant Address GE LUNAR CORP. 726 Heartland Trail madison, WI 53717

Supplemental Filings

Supplement NumberDateSupplement Type
P970040Original Filing
S003 2004-07-15 Normal 180 Day Track No User Fee
S002 2001-05-07 Normal 180 Day Track
S001 1999-02-16 Real-time Process

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