510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K973198Substantially Equivalent

Vgf-7 Vascular Graft Flowmeter

Medicard, Ltd., North Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973198 is the FDA 510(k) clearance record for VGF-7 VASCULAR GRAFT FLOWMETER, a class II device, cleared for Medicard , Ltd. on under FDA product code DPW (Flowmeter, Blood, Cardiovascular). FDA records list one 510(k) clearance for Medicard , Ltd. As of , FDA records show no recalls naming K973198.

Clearance record

Decision date
Received
(414 days to decision)
Product code
DPW Flowmeter, Blood, Cardiovascular
Regulation
21 CFR 870.2100
Device class
Class II
Review panel
Cardiovascular
Applicant
Medicard , Ltd. 49 Plain St., North Attleboro MA
510(k) summary
Summary
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