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FDA 510(k)

ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER

K-Number: K963185 · 1996-10-02

Decision Date1996-10-02
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER is the device name listed in this FDA 510(k) record. The listed applicant is Electronic Control Concepts. It received FDA 510(k) clearance on 1996-10-02 under 510(k) number K963185. 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 ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER?

ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER is a medical device that received FDA 510(k) clearance on 1996-10-02. The listed applicant is Electronic Control Concepts. The 510(k) number is K963185.

When did ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER receive FDA 510(k) clearance?

ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER received FDA 510(k) clearance on 1996-10-02, under 510(k) number K963185.

Who is the listed applicant for ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER?

The FDA 510(k) record lists Electronic Control Concepts as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER?

The FDA product code for ELECTRONIC X-RAY TIMER 1400A, 1400AW AND UNIVERSAL DIGITAL DENTAL X-RAY TIMER is EHD.

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.

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.

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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