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FDA 510(k)

INTEGRATED DISPLAY TECHNOLOGY LTD.

K-Number: K853130 · 1985-11-08

Decision Date1985-11-08
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTEGRATED DISPLAY TECHNOLOGY LTD. is the device name listed in this FDA 510(k) record. The listed applicant is Integrated Display Technology, Ltd.. It received FDA 510(k) clearance on 1985-11-08 under 510(k) number K853130. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRATED DISPLAY TECHNOLOGY LTD.?

INTEGRATED DISPLAY TECHNOLOGY LTD. is a medical device that received FDA 510(k) clearance on 1985-11-08. The listed applicant is Integrated Display Technology, Ltd.. The 510(k) number is K853130.

When did INTEGRATED DISPLAY TECHNOLOGY LTD. receive FDA 510(k) clearance?

INTEGRATED DISPLAY TECHNOLOGY LTD. received FDA 510(k) clearance on 1985-11-08, under 510(k) number K853130.

Who is the listed applicant for INTEGRATED DISPLAY TECHNOLOGY LTD.?

The FDA 510(k) record lists Integrated Display Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTEGRATED DISPLAY TECHNOLOGY LTD.?

The FDA product code for INTEGRATED DISPLAY TECHNOLOGY LTD. is FLL.

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.

Other records listing Integrated Display Technology, Ltd. 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.

Related Devices (Code: FLL)

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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