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

WEBRAD COMPUTED RADIOGRAPHY QUALITY ASSURANCE WORKSTATION

K Number: K991626 · Decision Jul 2, 1999
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
32
Review Days
52

Basic Information

Device Name
WEBRAD COMPUTED RADIOGRAPHY QUALITY ASSURANCE WORKSTATION
K Number
K991626
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ANALOGIC CORP.
Date Received
May 11, 1999
Decision Date
July 2, 1999
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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K043025 SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250
K041434 C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS
K041376 C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925A
K040995 SYNERAD MULTI DIGITAL X-RAY SYSTEM, MODEL AN6150
K033345 AN5150 AND AN7150 DIGITAL RADIOLOGY SYSTEMS
K030931 C3 PATIENT MONITOR
K011304 OB-1 FETAL MONITOR
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