510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K172296Substantially Equivalent

Stethee Pro

M3Dicine Pty, Ltd., Brisbane, AU / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K172296 is the FDA 510(k) clearance record for Stethee Pro, a class II device, cleared for M3Dicine Pty , Ltd. on under FDA product code DQD (Stethoscope, Electronic). FDA records list 2 510(k) clearances for M3Dicine Pty , Ltd., from to . As of , FDA records show no recalls naming K172296.

Clearance record

Decision date
Received
(91 days to decision)
Product code
DQD Stethoscope, Electronic
Regulation
21 CFR 870.1875
Device class
Class II
Review panel
Cardiovascular
Applicant
M3Dicine Pty , Ltd. 1389 Beenleigh Rd., Brisbane, AU
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code DQD

Trailing 12 months
6 clearances under product code DQD in the twelve months to October 2026, July 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DQD, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20260
July 20262
August 20260
September 20260
October 20260