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FDA 510(k)

LYELL SOUND

K-Number: K954972 · 1996-01-24

ApplicantVenture Management Corp.
Decision Date1996-01-24
Product CodeFBS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LYELL SOUND is the device name listed in this FDA 510(k) record. The listed applicant is Venture Management Corp.. It received FDA 510(k) clearance on 1996-01-24 under 510(k) number K954972. The device is classified under product code FBS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYELL SOUND?

LYELL SOUND is a medical device that received FDA 510(k) clearance on 1996-01-24. The listed applicant is Venture Management Corp.. The 510(k) number is K954972.

When did LYELL SOUND receive FDA 510(k) clearance?

LYELL SOUND received FDA 510(k) clearance on 1996-01-24, under 510(k) number K954972.

Who is the listed applicant for LYELL SOUND?

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

What is the FDA product code for LYELL SOUND?

The FDA product code for LYELL SOUND is FBS.

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.

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Other records listing Venture Management 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.

K943178DELTAK940848GELFLEX

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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