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

WINGED INFUSION SET

K Number: K902166 · Decision Aug 17, 1990
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
26
Review Days
94

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Basic Information

Device Name
WINGED INFUSION SET
K Number
K902166
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Therex Corp.
Date Received
May 15, 1990
Decision Date
August 17, 1990
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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K953110 LOW PROFILE TITANIUM MODEL CATALOG #1003
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K952537 THEREX LOW PROFILE TITANIUM MODEL 1.0MM I.D./1.8MM O.D.
K950212 A2 DETACHED DUAL PORT SYSTEM
K950131 1.0MM 1.8MMO.D. POLYURETHANE DETACHED MODEL
K942412 THEREX LOW-PROFILE PORT - TITANIUM MODEL
K934792 THEREX LOW-PROFILE PORT
K936012 THEREX LOW PROFILE PORT-TITANIUM MODEL
K934802 THEREX LOW-PROFILE PORT-TITANIUM
K933316 THEREX LOW-PROFILE PORT DETACHED CATHETER SYSTEM
Search all 26 clearances from Therex Corp. →