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

E-Z-EM PULSED INFUSION SYSTEM

K Number: K905447 · Decision Apr 1, 1991
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
174
Applicant Total
56
Review Days
117

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Basic Information

Device Name
E-Z-EM PULSED INFUSION SYSTEM
K Number
K905447
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
E-Z-Em, Inc.
Date Received
December 5, 1990
Decision Date
April 1, 1991
Product Code
KRA
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
KRA Catheter, Continuous Flush

Similar 510(k) Clearances

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Other Clearances by E-Z-Em, Inc.

K Number Device Name
K071378 MODIFICATION TO EMPOWER CT/CTA INJECTOR SYSTEM, MODELS 9800/9900 PRODUCT SERIES
K062449 EMPOWERMR INJECTOR SYSTEM, MODEL 9730
K063029 EMPOWER CT/CTA INJECTOR SYSTEM, MODEL 9800/9900
K053008 E-Z-EM ENDOSCOPIC CO2 REGULATOR
K041178 EMPOWER TRANSFER SET, (CAT. NO. 7725)
K031571 EMPOWERCTA INJECTOR SYSTEM, MODELS 9930 & 9910 & 9825
K030854 PROTOCO2L COLON INSUFFLATOR WITH PERFORMANCE IMPROVEMENTS, MODEL 6400
K013219 PROTOCO2L INSUFFLATOR MODEL 6400
K011160 E-Z EM PERCUPUMP 2001 CT INJECTOR
K974621 PERCUPUMP II WITH EDA
Search all 56 clearances from E-Z-Em, Inc. →