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

VERSACATH(TM0 MAINLINE(TM) WITH INTRODUCTION TRAY

K Number: K910564 · Decision May 6, 1991
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
31
Review Days
87

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Basic Information

Device Name
VERSACATH(TM0 MAINLINE(TM) WITH INTRODUCTION TRAY
K Number
K910564
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Menlo Care, Inc.
Date Received
February 8, 1991
Decision Date
May 6, 1991
Product Code
FOZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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Other Clearances by Menlo Care, Inc.

K Number Device Name
K964447 PICC CATHETER/MIDLINE CATHETER
K951620 MIDMARK MIDLINE CATHETER
K945521 CENTERMARK(R) PICC INSERTION TRAY LANDMARK(R) MIDLINE CATHETER PREP TRAY
K944968 LANDMARK MIDLINE CATHETER
K950737 LANDMARK MIDLINE CATHETER
K943893 PERCUTANEOUS GRAINAGE CATHETER
K943143 BILIARY STENT
K930048 SAFE-PICC CATHETER
K933941 MENLO CARE URINARY DIVERSION STENT
K940127 CENTERMARK SECURING WINGS
Search all 31 clearances from Menlo Care, Inc. →