510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K940236Substantially Equivalent

Quantitative Heart

Siemens Medical Solutions USA, Inc., Hoffman Estates IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940236 is the FDA 510(k) clearance record for QUANTITATIVE HEART, a class II device, cleared for Siemens Medical Solutions USA, Inc. on under FDA product code KPS (System, Tomography, Computed, Emission). FDA records list 829 510(k) clearances for Siemens Medical Solutions USA, Inc., from to . As of , FDA records show no recalls naming K940236.

Clearance record

Decision date
Received
(105 days to decision)
Product code
KPS System, Tomography, Computed, Emission
Regulation
21 CFR 892.1200
Device class
Class II
Review panel
Radiology
Applicant
Siemens Medical Solutions USA, Inc. Roentgen Angiography Chicago, Hoffman Estates IL
510(k) summary
Summary
Third party review
No

Clearances, product code KPS

Trailing 12 months
8 clearances under product code KPS in the twelve months to November 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KPS, trailing twelve months
MonthClearances
December 20252
January 20261
February 20261
March 20260
April 20261
May 20261
June 20260
July 20261
August 20260
September 20261
October 20260
November 20260