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

BIMECO FILTERED EXTENSION SET

K Number: K801605 · Decision Aug 12, 1980
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
41
Review Days
28

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Basic Information

Device Name
BIMECO FILTERED EXTENSION SET
K Number
K801605
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Burron Medical Products, Inc.
Date Received
July 15, 1980
Decision Date
August 12, 1980
Product Code
FPB
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
FPB Filter, Infusion Line

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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
K834299 LONG TERM CENTRAL VENOUS ACCESS CATH
K834473 MULTI-LUMEN CENTRAL VENOUS CATH. KIT
K840179 CONTINUOUS EPIDURAL ANESTHES. TRAY
Search all 41 clearances from Burron Medical Products, Inc. →