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FDA 510(k)

LYNX EL MICROSCOPY TISSUE PROCESSOR

K-Number: K862457 · 1986-07-16

Decision Date1986-07-16
Product CodeIDZ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

LYNX EL MICROSCOPY TISSUE PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Australian Biomedical Corporation , Ltd.. It received FDA 510(k) clearance on 1986-07-16 under 510(k) number K862457. The device is classified under product code IDZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYNX EL MICROSCOPY TISSUE PROCESSOR?

LYNX EL MICROSCOPY TISSUE PROCESSOR is a medical device that received FDA 510(k) clearance on 1986-07-16. The listed applicant is Australian Biomedical Corporation , Ltd.. The 510(k) number is K862457.

When did LYNX EL MICROSCOPY TISSUE PROCESSOR receive FDA 510(k) clearance?

LYNX EL MICROSCOPY TISSUE PROCESSOR received FDA 510(k) clearance on 1986-07-16, under 510(k) number K862457.

Who is the listed applicant for LYNX EL MICROSCOPY TISSUE PROCESSOR?

The FDA 510(k) record lists Australian Biomedical Corporation , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LYNX EL MICROSCOPY TISSUE PROCESSOR?

The FDA product code for LYNX EL MICROSCOPY TISSUE PROCESSOR is IDZ.

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 Australian Biomedical Corporation , Ltd. 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: IDZ)

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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