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

STRATO MEDICAL SINGLE LUMEN VALVED CATHETER

K Number: K924851 · Decision Dec 13, 1993
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
301
Applicant Total
45
Review Days
441

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Basic Information

Device Name
STRATO MEDICAL SINGLE LUMEN VALVED CATHETER
K Number
K924851
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Unknown
Statement or Summary
Summary
Applicant
Strato Medical Corp.
Date Received
September 28, 1992
Decision Date
December 13, 1993
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 Strato Medical Corp.

K Number Device Name
K945956 STRATO MEDICAL INFUSE-A-CATH TRIPLE LUMEN SILICONE CATHETER SYSTEMS
K946250 STRATO MEDICAL INFUSE-A-CATH, TRIPLE LUMEN POLYURETHANE, CENTRAL VNOUS CATHETER SYSTEMS
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
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
K924505 SNAP-LOCK MICROPORT - REVISED
Search all 45 clearances from Strato Medical Corp. →