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

I.V. START KIT

K Number: K924811 · Decision Jun 17, 1993
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
29
Applicant Total
21
Review Days
265

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Basic Information

Device Name
I.V. START KIT
K Number
K924811
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Unknown
Statement or Summary
Statement
Applicant
Transidyne General Corp.
Date Received
September 25, 1992
Decision Date
June 17, 1993
Product Code
LRS
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LRS I.V. Start Kit

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K950449 SURGICAL BUR
K950403 SURGICAL SAW BLADES
K924243 TRACHEOSTOMY CARE KIT
K922339 SUTURE REMOVAL KIT
K922041 PRIMARY SURGICAL DRESSING TRAY
K897133 MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT
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