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

CARDIUS-1 AND CARDIS-2

K Number: K030085 · Decision Feb 5, 2003
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
459
Applicant Total
13
Review Days
27

Basic Information

Device Name
CARDIUS-1 AND CARDIS-2
K Number
K030085
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DIGIRAD CORP.
Date Received
January 9, 2003
Decision Date
February 5, 2003
Product Code
KPS
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
KPS System, Tomography, Computed, Emission

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Other Clearances by DIGIRAD CORP.

K Number Device Name
K123408 ERGO IMAGING SYSTEM
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K083649 CARDIUS 3 X-ACT
K082904 STASYS MOTION CORRECTION SOFTWARE
K082368 CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM
K070542 CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS
K052430 CARDIUS-1, CARDIUS-2, CARDIUS-3, 2020TC SPECT IMAGING SYSTEM
K051549 CARDIUS-1, CARDIUS-2, CARDIUS-3, 2020TC SPECT IMAGING SYSTEM
K023110 CEDARS-SINAI MOTION CORRECTION (MOCO) SOFTWARE, MODEL 111005
K011572 QUANTITATIVE GATED SPECT (QGS), QUANTITATIVE PERFUSION SPECT (QPS)
Search all 13 clearances from DIGIRAD CORP. →