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FDA 510(k)

FIBER OPTIC HOSE

K-Number: K801592 · 1980-07-21

ApplicantLares Manufacturing Co., Inc.
Decision Date1980-07-21
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC HOSE is the device name listed in this FDA 510(k) record. The listed applicant is Lares Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K801592. 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 HOSE?

FIBER OPTIC HOSE is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Lares Manufacturing Co., Inc.. The 510(k) number is K801592.

When did FIBER OPTIC HOSE receive FDA 510(k) clearance?

FIBER OPTIC HOSE received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801592.

Who is the listed applicant for FIBER OPTIC HOSE?

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

What is the FDA product code for FIBER OPTIC HOSE?

The FDA product code for FIBER OPTIC HOSE is EAY.

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Other records listing Lares Manufacturing Co., 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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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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