510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K210811Substantially Equivalent

Dynamyx Digital Pathology Software

Inspirata, Inc., Tampa FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210811 is the FDA 510(k) clearance record for Dynamyx Digital Pathology Software, a class II device, cleared for Inspirata, Inc. on under FDA product code QKQ (Digital Pathology Image Viewing And Management Software). FDA's definition for product code QKQ reads: "Digital pathology image viewing and management software device is a software intended for viewing and management of digital images of scanned surgical pathology slides prepared from formalin-fixed paraffin embedded (FFPE) tissue. It is an...". FDA records list one 510(k) clearance for Inspirata, Inc. As of , FDA records show no recalls naming K210811.

Clearance record

Decision date
Received
(349 days to decision)
Product code
QKQ Digital Pathology Image Viewing And Management Software
Regulation
21 CFR 864.3700
Device class
Class II
Review panel
Pathology
Applicant
Inspirata, Inc. One N. Dale Mabry Hwy., Tampa FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QKQ

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