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

PICC CATHETER/MIDLINE CATHETER

K Number: K964447 · Decision Apr 16, 1997
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
301
Applicant Total
31
Review Days
161

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Basic Information

Device Name
PICC CATHETER/MIDLINE CATHETER
K Number
K964447
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Menlo Care, Inc.
Date Received
November 6, 1996
Decision Date
April 16, 1997
Product Code
LJS
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
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

Similar 510(k) Clearances

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

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Other Clearances by Menlo Care, Inc.

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