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

BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK

K Number: K013634 · Decision Jul 9, 2002
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
76
Applicant Total
11
Review Days
246

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Basic Information

Device Name
BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK
K Number
K013634
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Bioteque Corp.
Date Received
November 5, 2001
Decision Date
July 9, 2002
Product Code
FJK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

Similar 510(k) Clearances

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

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Other Clearances by Bioteque Corp.

K Number Device Name
K150932 Sheath Introducer
K102633 BIOTEQ ANGIOGRAPHIC CATHETER
K033862 BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY STRING LOCK
K033210 BIOTEQ DOUBLE PIGTAIL URETERAL STENT SET
K032292 BIOTEQUE A.V. FISTULA NEEDLE SET WITH SAFETY FLEX
K012526 BIOTEQUE SCALP VEIN SET
K002449 BIOTEQ I.V. (INTRAVENOUS) SET
K992930 BIOTEQUE HEMODIALYSIS BLOOD TUBING SET
K993118 BIOTEQUE A.V. FISTULA NEEDLE SET
K915491 CURELLE
Search all 11 clearances from Bioteque Corp. →