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FDA 510(k)

FIBER OPTIC LIGHT SOURCE I

K-Number: K812605 · 1981-10-02

ApplicantVenture Technology, Inc.
Decision Date1981-10-02
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC LIGHT SOURCE I is the device name listed in this FDA 510(k) record. The listed applicant is Venture Technology, Inc.. It received FDA 510(k) clearance on 1981-10-02 under 510(k) number K812605. The device is classified under product code EAY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER OPTIC LIGHT SOURCE I?

FIBER OPTIC LIGHT SOURCE I is a medical device that received FDA 510(k) clearance on 1981-10-02. The listed applicant is Venture Technology, Inc.. The 510(k) number is K812605.

When did FIBER OPTIC LIGHT SOURCE I receive FDA 510(k) clearance?

FIBER OPTIC LIGHT SOURCE I received FDA 510(k) clearance on 1981-10-02, under 510(k) number K812605.

Who is the listed applicant for FIBER OPTIC LIGHT SOURCE I?

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

What is the FDA product code for FIBER OPTIC LIGHT SOURCE I?

The FDA product code for FIBER OPTIC LIGHT SOURCE I is EAY.

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Other records listing Venture Technology, Inc. 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.

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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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