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

VASCULAR ACCESS CATHETER

K Number: K851195 · Decision Jun 7, 1985
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
301
Applicant Total
29
Review Days
73

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Basic Information

Device Name
VASCULAR ACCESS CATHETER
K Number
K851195
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Sil-Med Corp.
Date Received
March 26, 1985
Decision Date
June 7, 1985
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 Sil-Med Corp.

K Number Device Name
K972521 NAVIGATOR (STYLET) 2006
K961392 ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II
K961194 ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN
K961295 SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR
K960099 PENROSE DRAIN MODELS 6001 - 6007
K955463 GRIP-A-BOOTS
K942709 MEDIASTINAL SILICONE DRAINS
K926496 SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN
K926408 SIL-SLIP FLAT SUCTION DRAIN
K926495 SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE
Search all 29 clearances from Sil-Med Corp. →