510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K252076Substantially Equivalent

Kneevoice Cartilage Evaluation System (750-3600-001)

Kneevoice, Inc., Santa Monica CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K252076 is the FDA 510(k) clearance record for Kneevoice Cartilage Evaluation System (750-3600-001), a class II device, cleared for Kneevoice, Inc. on under FDA product code DQD (Stethoscope, Electronic). FDA records list one 510(k) clearance for Kneevoice, Inc. As of , FDA records show no recalls naming K252076.

Clearance record

Decision date
Received
(219 days to decision)
Product code
DQD Stethoscope, Electronic
Regulation
21 CFR 870.1875
Device class
Class II
Review panel
Cardiovascular
Applicant
Kneevoice, Inc. 1626 Montana Ave., Santa Monica CA
510(k) summary
Summary PDF
Third party review
No

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