510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K861241Substantially Equivalent

Angiotopo Catheter

Houston Biomedical, Inc., Houston TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K861241 is the FDA 510(k) clearance record for ANGIOTOPO CATHETER, a class II device, cleared for Houston Biomedical, Inc. on under FDA product code DQO (Catheter, Intravascular, Diagnostic). FDA records list 3 510(k) clearances for Houston Biomedical, Inc., from to . As of , FDA records show no recalls naming K861241.

Clearance record

Decision date
Received
(279 days to decision)
Product code
DQO Catheter, Intravascular, Diagnostic
Regulation
21 CFR 870.1200
Device class
Class II
Review panel
Cardiovascular
Applicant
Houston Biomedical, Inc. 1900 Yorktown Suite 400, Houston TX
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