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FDA 510(k)

LIQUID CRYSTAL DISPLAY DIGITAL WATCH

K-Number: K780445 · 1978-06-19

ApplicantHughes Aircraft Co.
Decision Date1978-06-19
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIQUID CRYSTAL DISPLAY DIGITAL WATCH is the device name listed in this FDA 510(k) record. The listed applicant is Hughes Aircraft Co.. It received FDA 510(k) clearance on 1978-06-19 under 510(k) number K780445. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CRYSTAL DISPLAY DIGITAL WATCH?

LIQUID CRYSTAL DISPLAY DIGITAL WATCH is a medical device that received FDA 510(k) clearance on 1978-06-19. The listed applicant is Hughes Aircraft Co.. The 510(k) number is K780445.

When did LIQUID CRYSTAL DISPLAY DIGITAL WATCH receive FDA 510(k) clearance?

LIQUID CRYSTAL DISPLAY DIGITAL WATCH received FDA 510(k) clearance on 1978-06-19, under 510(k) number K780445.

Who is the listed applicant for LIQUID CRYSTAL DISPLAY DIGITAL WATCH?

The FDA 510(k) record lists Hughes Aircraft Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUID CRYSTAL DISPLAY DIGITAL WATCH?

The FDA product code for LIQUID CRYSTAL DISPLAY DIGITAL WATCH is DRT.

Related Clinical Trials

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Other records listing Hughes Aircraft Co. 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.

K843549PROBEYE THERMAL VIDEO SYSTEMS

Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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