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

DUAL LUMEN CATHETER

K Number: K043581 · Decision Mar 3, 2005
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
27
Applicant Total
16
Review Days
65

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Basic Information

Device Name
DUAL LUMEN CATHETER
K Number
K043581
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acmi Corporation
Date Received
December 28, 2004
Decision Date
March 3, 2005
Product Code
EYB
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
EYB Catheter, Ureteral, Gastro-Urology

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Other Clearances by Acmi Corporation

K Number Device Name
K061975 PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK
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K060269 ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM
K051593 UROPASS URETERAL ACCESS SHEATH, MODEL 61224
K052044 ACMI AUTOCLAVABLE URETEROSCOPE, MODELS MR-6A AND MR-6AL
K042069 INVISIO IRL DIGITAL RIGID LAPAROSCOPE SYSTEM
K042225 ACMI INVISIO ICN, MODELS ICN-0564 AND ICN-0565
K031758 ACMI M4 TELESCOPES
K030960 ECN ELECTRONIC VIDEO CYSTONEPHROSCOPE
K030935 BERKELEY V-10 VACUUM CURETTAGE SYSTEM
Search all 16 clearances from Acmi Corporation →