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FDA 510(k) Application Details - K980091
Device Classification Name
Transducer, Ultrasonic, Diagnostic
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510(K) Number
K980091
Device Name
Transducer, Ultrasonic, Diagnostic
Applicant
COSMACEUTICAL MARKETING, INC.
10820 ALDER CIR.
DALLAS, TX 75238 US
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Contact
MICHAEL CASWELL
Other 510(k) Applications for this Contact
Regulation Number
892.1570
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Classification Product Code
ITX
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More FDA Info for this Product Code
Date Received
01/09/1998
Decision Date
04/09/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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