510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K922034Substantially Equivalent

Lv-20 Volumeter, 20 Mhz Doppler Blood Flow Meter

Titronics Medical Instruments, Inc., Iowa City IA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K922034 is the FDA 510(k) clearance record for LV-20 VOLUMETER, 20 MHZ DOPPLER BLOOD FLOW METER, a class II device, cleared for Titronics Medical Instruments, Inc. on under FDA product code DPW (Flowmeter, Blood, Cardiovascular). FDA records list 2 510(k) clearances for Titronics Medical Instruments, Inc., from to . As of , FDA records show no recalls naming K922034.

Clearance record

Decision date
Received
(382 days to decision)
Product code
DPW Flowmeter, Blood, Cardiovascular
Regulation
21 CFR 870.2100
Device class
Class II
Review panel
Cardiovascular
Applicant
Titronics Medical Instruments, Inc. P.O. Box 2202, Iowa City IA
510(k) summary
Statement
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