510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K173187Substantially Equivalent

MobileDiagnost M50

Philips India Limited, Pune, IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K173187 is the FDA 510(k) clearance record for MobileDiagnost M50, a class II device, cleared for Philips India Limited on under FDA product code IZL (System, X-Ray, Mobile). FDA records list 2 510(k) clearances for Philips India Limited, from to . As of , FDA records show no recalls naming K173187.

Clearance record

Decision date
Received
(45 days to decision)
Product code
IZL System, X-Ray, Mobile
Regulation
21 CFR 892.1720
Device class
Class II
Review panel
Radiology
Applicant
Philips India Limited Plot # B-79, Midc, Phase Ii, Chakan, Taluka-Khed, Pune, IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IZL

Trailing 12 months
6 clearances under product code IZL in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code IZL, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20261
July 20260
August 20261
September 20260
October 20260