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

BIOTEQUE SCALP VEIN SET

K Number: K012526 · Decision Sep 14, 2001
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
11
Review Days
39

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Basic Information

Device Name
BIOTEQUE SCALP VEIN SET
K Number
K012526
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bioteque Corp.
Date Received
August 6, 2001
Decision Date
September 14, 2001
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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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
K013634 BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK
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. →