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FDA 510(k)

ELDER PSORALITE, SERIES 43000

K-Number: K837105 · 1983-03-07

Decision Date1983-03-07
Product Code
DecisionSubstantially Equivalent

Device Summary

ELDER PSORALITE, SERIES 43000 is the device name listed in this FDA 510(k) record. The listed applicant is Elder Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1983-03-07 under 510(k) number K837105. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELDER PSORALITE, SERIES 43000?

ELDER PSORALITE, SERIES 43000 is a medical device that received FDA 510(k) clearance on 1983-03-07. The listed applicant is Elder Pharmaceuticals, Inc.. The 510(k) number is K837105.

When did ELDER PSORALITE, SERIES 43000 receive FDA 510(k) clearance?

ELDER PSORALITE, SERIES 43000 received FDA 510(k) clearance on 1983-03-07, under 510(k) number K837105.

Who is the listed applicant for ELDER PSORALITE, SERIES 43000?

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

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 Elder Pharmaceuticals, 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.

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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