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

LONG TERM CENTRAL VENOUS ACCESS CATH

K Number: K834299 · Decision May 1, 1984
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
301
Applicant Total
41
Review Days
145

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Basic Information

Device Name
LONG TERM CENTRAL VENOUS ACCESS CATH
K Number
K834299
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Burron Medical Products, Inc.
Date Received
December 8, 1983
Decision Date
May 1, 1984
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

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Other Clearances by Burron Medical Products, Inc.

K Number Device Name
K870403 CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTURE
K862412 INTESTOPLANT
K861479 CAVAFIX, CENTRAL VENOUS CATHETER KIT
K860126 STIMUPLEX, NERVE STIMULATOR
K851293 IMPLANTOFIX
K841428 JEJUNOSTOMY SET FOR TUBE FEEDING
K834383 DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT
K834473 MULTI-LUMEN CENTRAL VENOUS CATH. KIT
K840179 CONTINUOUS EPIDURAL ANESTHES. TRAY
K840287 BRACHIAL PLEXUS ANESTHESIA TRAY
Search all 41 clearances from Burron Medical Products, Inc. →