FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

SAFE-PICC PERIPHERALLY INSERTED CENTRAL VENOUS CAT

K Number: K920828 · Decision Aug 14, 1992
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
31
Review Days
172

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Basic Information

Device Name
SAFE-PICC PERIPHERALLY INSERTED CENTRAL VENOUS CAT
K Number
K920828
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Unknown
Statement or Summary
Statement
Applicant
Menlo Care, Inc.
Date Received
February 24, 1992
Decision Date
August 14, 1992
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

Similar 510(k) Clearances

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

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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. →