510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K222781Substantially Equivalent

Augmento

Deeptek Medical Imaging Private Limited, Pune, IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K222781 is the FDA 510(k) clearance record for Augmento, a class II device, cleared for Deeptek Medical Imaging Private Limited on under FDA product code LLZ (System, Image Processing, Radiological). FDA records list one 510(k) clearance for Deeptek Medical Imaging Private Limited. As of , FDA records show no recalls naming K222781.

Clearance record

Decision date
Received
(208 days to decision)
Product code
LLZ System, Image Processing, Radiological
Regulation
21 CFR 892.2050
Device class
Class II
Review panel
Radiology
Applicant
Deeptek Medical Imaging Private Limited 3rd Floor, Ideas To Impact, Pallod Farms 3, Baner, Pune, IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LLZ

Trailing 12 months
48 clearances under product code LLZ in the twelve months to October 2026, July 2026 the highest month at 8.
Show the numbers
Monthly 510(k) clearances under FDA product code LLZ, trailing twelve months
MonthClearances
November 20254
December 20251
January 20263
February 20264
March 20266
April 20262
May 20265
June 20265
July 20268
August 20263
September 20267
October 20260