510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K231001Substantially Equivalent

DeepTek CXR Analyzer v1.0

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

K231001 is the FDA 510(k) clearance record for DeepTek CXR Analyzer v1.0, a class II device, cleared for Deeptek Medical Imaging Pvt, Ltd. on under FDA product code MYN (Analyzer, Medical Image). FDA's definition for product code MYN reads: "For information on the MYN device, please see: https://www.federalregister.gov/documents/2020/01/22/2020-00494/radiology-devices-reclassification-of-medical-image-analyzers". FDA records list one 510(k) clearance for Deeptek Medical Imaging Pvt, Ltd. As of , FDA records show no recalls naming K231001.

Clearance record

Decision date
Received
(181 days to decision)
Product code
MYN Analyzer, Medical Image
Regulation
21 CFR 892.2070
Device class
Class II
Review panel
Radiology
Applicant
Deeptek Medical Imaging Pvt, Ltd. 3rd Floor, Ideas To Impact, Pallod Farms 3, Pune, IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MYN

Trailing 12 months
10 clearances under product code MYN in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code MYN, trailing twelve months
MonthClearances
November 20253
December 20250
January 20263
February 20260
March 20260
April 20260
May 20261
June 20260
July 20261
August 20261
September 20261
October 20260