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FDA 510(k)

JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002

K-Number: K020070 · 2002-02-01

ApplicantProgeny, Inc.
Decision Date2002-02-01
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002 is the device name listed in this FDA 510(k) record. The listed applicant is Progeny, Inc.. It received FDA 510(k) clearance on 2002-02-01 under 510(k) number K020070. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002?

JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002 is a medical device that received FDA 510(k) clearance on 2002-02-01. The listed applicant is Progeny, Inc.. The 510(k) number is K020070.

When did JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002 receive FDA 510(k) clearance?

JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002 received FDA 510(k) clearance on 2002-02-01, under 510(k) number K020070.

Who is the listed applicant for JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002?

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 JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002?

The FDA product code for JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002 is EHD.

Related Clinical Trials

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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, P7015K041831PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR

Related Devices (Code: EHD)

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.

K260795Hand-held Dental X-ray System (HyperLight-M)Changzhou Sifary Medical Technology Co., Ltd.K260367Portable Dental X-ray System Model PDX novaPDX Co., Ltd.K253864NOMAD Pro 3Dental Imaging Technologies CorporationK252110Dental X-RAY Unit (AJX200)Guangzhou Ajax Medical Equipment Co., Ltd.K254018Portable Dental X-ray Device (GT-1)Guilin Refine Medical Instrument Co., Ltd.K252909Diagnostic X-Ray Equipment Model POCT22Ningbo Runyes Medical Instrument Co., Ltd.

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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