FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CENTERMARK SECURING WINGS

K Number: K940127 · Decision Feb 9, 1994
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
63
Applicant Total
31
Review Days
30

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Basic Information

Device Name
CENTERMARK SECURING WINGS
K Number
K940127
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5210
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Menlo Care, Inc.
Date Received
January 10, 1994
Decision Date
February 9, 1994
Product Code
KMK
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
KMK Device, Intravascular Catheter Securement

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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
K923394 MENLO CARE AQUASTENT SET
Search all 31 clearances from Menlo Care, Inc. →