510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K013634Unknown

Bioteque 3 in 1 Hemodialysis Blood Tubing Pack

Bioteque Corp., Flagstaff AZ / Traditional, Unknown
FDA source (opens on fda.gov)

K013634 is the FDA 510(k) clearance record for BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK, a class II device, cleared for Bioteque Corp. on under FDA product code FJK (Set, Tubing, Blood, With And Without Anti-Regurgitation Valve). FDA records list 14 510(k) clearances for Bioteque Corp., from to . As of , FDA records show no recalls naming K013634.

Clearance record

Decision date
Received
(246 days to decision)
Product code
FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Bioteque Corp. 3892 S. America W. Trl., Flagstaff AZ
510(k) summary
Summary
Third party review
No

Clearances, product code FJK

Trailing 12 months
2 clearances under product code FJK in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FJK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260