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

E-Z-EM ENTEROCLYSIS CATHETER SET

K Number: K911349 · Decision Nov 16, 1992
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
2
Applicant Total
56
Review Days
600

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Basic Information

Device Name
E-Z-EM ENTEROCLYSIS CATHETER SET
K Number
K911349
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
E-Z-Em, Inc.
Date Received
March 27, 1991
Decision Date
November 16, 1992
Product Code
EZK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
EZK Catheter, Retention Type

Similar 510(k) Clearances

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

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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. →