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FDA 510(k)

DIGITAL VIDEO RECORDING SYSTEM

K-Number: K991738 · 1999-08-13

ApplicantKay Elemetrics Corp.
Decision Date1999-08-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL VIDEO RECORDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Kay Elemetrics Corp.. It received FDA 510(k) clearance on 1999-08-13 under 510(k) number K991738. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL VIDEO RECORDING SYSTEM?

DIGITAL VIDEO RECORDING SYSTEM is a medical device that received FDA 510(k) clearance on 1999-08-13. The listed applicant is Kay Elemetrics Corp.. The 510(k) number is K991738.

When did DIGITAL VIDEO RECORDING SYSTEM receive FDA 510(k) clearance?

DIGITAL VIDEO RECORDING SYSTEM received FDA 510(k) clearance on 1999-08-13, under 510(k) number K991738.

Who is the listed applicant for DIGITAL VIDEO RECORDING SYSTEM?

The FDA 510(k) record lists Kay Elemetrics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL VIDEO RECORDING SYSTEM?

The FDA product code for DIGITAL VIDEO RECORDING SYSTEM is LLZ.

Related Clinical Trials

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Other records listing Kay Elemetrics Corp. 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.

K990240ELECTROGLOTTOGRAPHK9547987100 SWALLOWING WORKSTATIONK9212859105 RIGID TELESCOPIC ENDOSCOPEK921184RLS 9100 RHINO-LARYNGEAL STROBOSCOPE

Related Devices (Code: LLZ)

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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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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