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

BLADDERSCAN BVI 6100

K Number: K022153 · Decision Aug 15, 2002
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
16
Review Days
44

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Basic Information

Device Name
BLADDERSCAN BVI 6100
K Number
K022153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostic Ultrasound Corp.
Date Received
July 2, 2002
Decision Date
August 15, 2002
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

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

Product Code Device Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

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K Number Device Name
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K963585 BLADDER MANAGER PCI 5000, BLADDERSCAN BVI 5000
K955840 BLADDERMANAGER PCI 5000 / BLADDERSCAN BVI 5000
K955942 BLADDERSCAN BVI 5000
K920664 DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020, GI VERSION
K915342 UD 2000 VIDEO OPTION
K915436 BLADDERSCAN BVI 2500
K911166 DIAGNOSTIC ULTRASOUND/URO-GYN UD 511
K911125 DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020
Search all 16 clearances from Diagnostic Ultrasound Corp. →