510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K970573Substantially Equivalent

Flexart V3.5 Software

Toshiba America Mri, Inc., S. San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970573 is the FDA 510(k) clearance record for FLEXART V3.5 SOFTWARE, a class II device, cleared for Toshiba America Mri, Inc. on under FDA product code LNH (System, Nuclear Magnetic Resonance Imaging). FDA records list 68 510(k) clearances for Toshiba America Mri, Inc., from to . As of , FDA records show no recalls naming K970573.

Clearance record

Decision date
Received
(157 days to decision)
Product code
LNH System, Nuclear Magnetic Resonance Imaging
Regulation
21 CFR 892.1000
Device class
Class II
Review panel
Radiology
Applicant
Toshiba America Mri, Inc. 280 Utah Ave., S. San Francisco CA
510(k) summary
Summary
Third party review
No

Clearances, product code LNH

Trailing 12 months
25 clearances under product code LNH in the twelve months to October 2026, March 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code LNH, trailing twelve months
MonthClearances
November 20251
December 20253
January 20261
February 20264
March 20266
April 20261
May 20261
June 20260
July 20262
August 20263
September 20263
October 20260