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FDA 510(k)

MODEL LC-85 UV DETECTOR

K-Number: K810304 · 1981-02-25

Decision Date1981-02-25
Product CodeLDM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL LC-85 UV DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1981-02-25 under 510(k) number K810304. The device is classified under product code LDM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL LC-85 UV DETECTOR?

MODEL LC-85 UV DETECTOR is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K810304.

When did MODEL LC-85 UV DETECTOR receive FDA 510(k) clearance?

MODEL LC-85 UV DETECTOR received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810304.

Who is the listed applicant for MODEL LC-85 UV DETECTOR?

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

What is the FDA product code for MODEL LC-85 UV DETECTOR?

The FDA product code for MODEL LC-85 UV DETECTOR is LDM.

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 The Perkin-Elmer 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.

View all 62 devices →

Related Devices (Code: LDM)

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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