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FDA 510(k)

LYSOCOLOR

K-Number: K860321 · 1986-02-20

Decision Date1986-02-20
Product CodeLED
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LYSOCOLOR is the device name listed in this FDA 510(k) record. The listed applicant is Cytocolor, Inc.. It received FDA 510(k) clearance on 1986-02-20 under 510(k) number K860321. The device is classified under product code LED. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYSOCOLOR?

LYSOCOLOR is a medical device that received FDA 510(k) clearance on 1986-02-20. The listed applicant is Cytocolor, Inc.. The 510(k) number is K860321.

When did LYSOCOLOR receive FDA 510(k) clearance?

LYSOCOLOR received FDA 510(k) clearance on 1986-02-20, under 510(k) number K860321.

Who is the listed applicant for LYSOCOLOR?

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

What is the FDA product code for LYSOCOLOR?

The FDA product code for LYSOCOLOR is LED.

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.

Other records listing Cytocolor, 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.

Related Devices (Code: LED)

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.

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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