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

THEREX LOW-PROFILE PORT-TITANIUM

K Number: K934802 · Decision Mar 22, 1994
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
287
Applicant Total
26
Review Days
166

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Basic Information

Device Name
THEREX LOW-PROFILE PORT-TITANIUM
K Number
K934802
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5965
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Therex Corp.
Date Received
October 7, 1993
Decision Date
March 22, 1994
Product Code
LJT
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
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LJT), ordered by most recent decision date.

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Other Clearances by Therex Corp.

K Number Device Name
K953110 LOW PROFILE TITANIUM MODEL CATALOG #1003
K953017 LOW PROFILE TITANIUM MODEL CATALOG #1003
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
K933316 THEREX LOW-PROFILE PORT DETACHED CATHETER SYSTEM
K933350 THEREX LOW-PROFILE PORT 1.5MM I.D. X 2.7MM O.D. DETACHED CATHETER SYSTEM
Search all 26 clearances from Therex Corp. →