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FDA 510(k)

UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W

K-Number: K111305 · 2012-01-31

ApplicantMeridian Medical Systems, LLC
Decision Date2012-01-31
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Medical Systems, LLC. It received FDA 510(k) clearance on 2012-01-31 under 510(k) number K111305. 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 UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W?

UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W is a medical device that received FDA 510(k) clearance on 2012-01-31. The listed applicant is Meridian Medical Systems, LLC. The 510(k) number is K111305.

When did UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W receive FDA 510(k) clearance?

UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W received FDA 510(k) clearance on 2012-01-31, under 510(k) number K111305.

Who is the listed applicant for UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W?

The FDA 510(k) record lists Meridian Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W?

The FDA product code for UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W is MQB.

Related Clinical Trials

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Other records listing Meridian Medical Systems, LLC as applicant

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.

K162687Paragon 2K112527UNIVERSAL DIGITAL INTERFACE (UDI) 1717K103599UNIVERSAL DIGITAL INTERFACE (UDI) 1717

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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