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

ZARGIS ACOUSTIC CARDIOSCAN

K Number: K031517 · Decision May 26, 2004
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
153
Applicant Total
5
Review Days
377

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Basic Information

Device Name
ZARGIS ACOUSTIC CARDIOSCAN
K Number
K031517
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zargis Medical Corp.
Date Received
May 15, 2003
Decision Date
May 26, 2004
Product Code
DQD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQD Stethoscope, Electronic

Similar 510(k) Clearances

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

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Other Clearances by Zargis Medical Corp.

K Number Device Name
K090493 SIGNAL
K083309 ZARGIS ACOUSTIC CARDIOSCAN, VERSION 9.33
K060197 ZARGIS ACOUSTIC CARDIOSCAN (ZAC), MODEL ZAC 6.28
K042128 MODIFICATION TO ZARGIS ACOUSTIC CARDIOSCAN (ZAC)