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

RAPID ADD SITE DOUBLE LUMEN I.V.EXTENSION SET

K Number: K915109 · Decision May 8, 1992
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
26
Review Days
177

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Basic Information

Device Name
RAPID ADD SITE DOUBLE LUMEN I.V.EXTENSION SET
K Number
K915109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ballard Medical Products
Date Received
November 13, 1991
Decision Date
May 8, 1992
Product Code
FPA
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
FPA Set, Administration, Intravascular

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K013892 LUTZ NEEDLE
K000495 BALLARD MEDICAL PRODUCTS EPIDURAL AND SPINAL NEEDLES
K993138 BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT
K990376 BALLARD MEDICAL PRODUCTS FACILETOME BOW STRING PAPILLOTOME
K982894 MIC-KEY GLOW PROFILE GASTROSTOMY REPLACEMENT KIT
K974630 72 HOUR USE TRACH CARE WITH MICROBAN
K964369 TRACH CARE SET WITH MICROBAN
K951533 EASI-LAV PEDIATRIC / ADULT GASTRIC LAVAGE KIT
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