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FDA 510(k)

WIRELESS PORTABLE DETECTOR FD-W17

K-Number: K090625 · 2009-03-24

ApplicantPhilips Medical Systems North America Co.
Decision Date2009-03-24
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WIRELESS PORTABLE DETECTOR FD-W17 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America Co.. It received FDA 510(k) clearance on 2009-03-24 under 510(k) number K090625. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIRELESS PORTABLE DETECTOR FD-W17?

WIRELESS PORTABLE DETECTOR FD-W17 is a medical device that received FDA 510(k) clearance on 2009-03-24. The listed applicant is Philips Medical Systems North America Co.. The 510(k) number is K090625.

When did WIRELESS PORTABLE DETECTOR FD-W17 receive FDA 510(k) clearance?

WIRELESS PORTABLE DETECTOR FD-W17 received FDA 510(k) clearance on 2009-03-24, under 510(k) number K090625.

Who is the listed applicant for WIRELESS PORTABLE DETECTOR FD-W17?

The FDA 510(k) record lists Philips Medical Systems North America Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIRELESS PORTABLE DETECTOR FD-W17?

The FDA product code for WIRELESS PORTABLE DETECTOR FD-W17 is MQB.

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Other records listing Philips Medical Systems North America Co. as applicant

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Related Devices (Code: MQB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K2538000909FCE, 0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 detector (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211Yushan X-Ray Flat Panel DetectorInnocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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