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

HYDRAVIEW 1000 DIGITAL IMAGE PROCESS/STOR DEVICE

K Number: K913264 · Decision Nov 1, 1991
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
27
Review Days
101

Basic Information

Device Name
HYDRAVIEW 1000 DIGITAL IMAGE PROCESS/STOR DEVICE
K Number
K913264
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
MALLINCKRODT GROUP, INC.
Date Received
July 23, 1991
Decision Date
November 1, 1991
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

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