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

STRATO PORT INTRODUCER KT(12 FR) LPS 5213/MODIFIED

K Number: K905842 · Decision Apr 19, 1991
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
285
Applicant Total
45
Review Days
113

Basic Information

Device Name
STRATO PORT INTRODUCER KT(12 FR) LPS 5213/MODIFIED
K Number
K905842
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5965
Medical Specialty
General Hospital
Decision
Unknown
Applicant
STRATO MEDICAL CORP.
Date Received
December 27, 1990
Decision Date
April 19, 1991
Product Code
LJT
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
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

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K942848 STRATO MEDICAL LIFEPORT LPS 7515
K934518 STRATO MEDICAL INFUSE-A-PORT/INFUSE-A-KIT PERIPORT PERIPHERAL ACCESS SYSTEM
K932509 STRATO MEDICAL INFUSE-A-PORT/SNAP-LOCK MACROPRORT
K933884 STRATO MEDICAL LIFEPORT LPS 7255 LOW PROFILE DUAL LUMEN VASCULAR ACCESS SYSTEM
K924851 STRATO MEDICAL SINGLE LUMEN VALVED CATHETER
K924677 STRATO MEDICAL INFUSE-A-CATH POLYURE CEN VEN CATH
K921751 INFUSE-A-CATH SILICONE CENTRAL VENOUS CATHETER
K915273 LIFEPORT ATTACHABLE SYSTEM W/INDUCER KIT LPS 5555
Search all 45 clearances from STRATO MEDICAL CORP. →