510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K090625Substantially Equivalent

Wireless Portable Detector Fd-W17

Philips North America LLC, Bothell WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K090625 is the FDA 510(k) clearance record for WIRELESS PORTABLE DETECTOR FD-W17, a class II device, cleared for Philips Medical Systems North America Co. on under FDA product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show 28 recalls naming K090625.

Clearance record

Decision date
Received
(15 days to decision)
Product code
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Regulation
21 CFR 892.1680
Device class
Class II
Review panel
Radiology
Applicant
Philips Medical Systems North America Co. 22100 Bothell Everett Hwy., Bothell WA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code MQB

Trailing 12 months
3 clearances under product code MQB in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MQB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20261
August 20260
September 20260
October 20260