510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K102633Substantially Equivalent

Bioteq Angiographic Catheter

Bioteque Corp., Flagstaff AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K102633 is the FDA 510(k) clearance record for BIOTEQ ANGIOGRAPHIC CATHETER, a class II device, cleared for Bioteque Corp. on under FDA product code DQO (Catheter, Intravascular, Diagnostic). FDA records list 14 510(k) clearances for Bioteque Corp., from to . As of , FDA records show no recalls naming K102633.

Clearance record

Decision date
Received
(361 days to decision)
Product code
DQO Catheter, Intravascular, Diagnostic
Regulation
21 CFR 870.1200
Device class
Class II
Review panel
Cardiovascular
Applicant
Bioteque Corp. 2904 N. Boldt Dr., Flagstaff AZ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQO

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