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

UD 2000 VIDEO OPTION

K Number: K915342 · Decision Jun 10, 1992
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
16
Review Days
197

Basic Information

Device Name
UD 2000 VIDEO OPTION
K Number
K915342
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DIAGNOSTIC ULTRASOUND CORP.
Date Received
November 26, 1991
Decision Date
June 10, 1992
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

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

View all

Other Clearances by DIAGNOSTIC ULTRASOUND CORP.

K Number Device Name
K030763 DIAGNOSTIC ULTRASOUND BLADDERMASS BVM 6500 ULTRASOUND SYSTEM
K022153 BLADDERSCAN BVI 6100
K982568 BLADDERMANAGER PCI 5000 MODEL 1002
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
K915436 BLADDERSCAN BVI 2500
K911125 DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020
K911166 DIAGNOSTIC ULTRASOUND/URO-GYN UD 511
Search all 16 clearances from DIAGNOSTIC ULTRASOUND CORP. →