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FDA 510(k)

PODIATRY X-RAY UNIT

K-Number: K827816 · 1982-08-24

Decision Date1982-08-24
Product Code
DecisionSubstantially Equivalent

Device Summary

PODIATRY X-RAY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is The S. S. White Co.. It received FDA 510(k) clearance on 1982-08-24 under 510(k) number K827816. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PODIATRY X-RAY UNIT?

PODIATRY X-RAY UNIT is a medical device that received FDA 510(k) clearance on 1982-08-24. The listed applicant is The S. S. White Co.. The 510(k) number is K827816.

When did PODIATRY X-RAY UNIT receive FDA 510(k) clearance?

PODIATRY X-RAY UNIT received FDA 510(k) clearance on 1982-08-24, under 510(k) number K827816.

Who is the listed applicant for PODIATRY X-RAY UNIT?

The FDA 510(k) record lists The S. S. White Co. 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 The S. S. White Co. 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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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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