510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K201114Substantially Equivalent

Bidop 7

Koven Technology, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K201114 is the FDA 510(k) clearance record for Bidop 7, a class II device, cleared for Koven Technology, Inc. on under FDA product code DPW (Flowmeter, Blood, Cardiovascular). FDA records list 18 510(k) clearances for Koven Technology, Inc., from to . As of , FDA records show no recalls naming K201114.

Clearance record

Decision date
Received
(253 days to decision)
Product code
DPW Flowmeter, Blood, Cardiovascular
Regulation
21 CFR 870.2100
Device class
Class II
Review panel
Cardiovascular
Applicant
Koven Technology, Inc. 477 N. Lindbergh Blvd., Suite 220, St. Louis MO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DPW

Trailing 12 months
3 clearances under product code DPW in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DPW, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260