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FDA 510(k)

PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR

K-Number: K041831 · 2004-08-09

ApplicantProgeny, Inc.
Decision Date2004-08-09
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Progeny, Inc.. It received FDA 510(k) clearance on 2004-08-09 under 510(k) number K041831. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR?

PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR is a medical device that received FDA 510(k) clearance on 2004-08-09. The listed applicant is Progeny, Inc.. The 510(k) number is K041831.

When did PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR receive FDA 510(k) clearance?

PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR received FDA 510(k) clearance on 2004-08-09, under 510(k) number K041831.

Who is the listed applicant for PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR?

The FDA 510(k) record lists Progeny, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR?

The FDA product code for PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR is MUH.

Related Clinical Trials

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.

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Other records listing Progeny, Inc. 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.

K090079VIVID, MODELS 40-A0001, 40-A0004, 40-A0006K070664PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).K043092PREVA, 76IN ARM, 66IN ARM, 56IN ARM, MODELS P7017, P7016, P7015K020070JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002

Related Devices (Code: MUH)

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.

K251793SOTA Cloud Smart Sensor (1.5)Sota Cloud Corp.K252570EzSensor HD, EzSensor UHDQpix Solutions, Inc.K250687Cocoon Solo (DX-7020s)Dexcowin Global, Inc.K251206Digital X-Ray DentiMax Pro Imaging SystemDentimax, Inc.K240040VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)VATECH Co., Ltd.K242778X Sensor (Model: IOS-A15IF, HDI-15DGF)Qpix Solutions, Inc.

Official Source

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

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