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FDA 510(k)

DENTAL CASSETTE HOLDERS

K-Number: K837515 · 1983-06-28

ApplicantXre Corp.
Decision Date1983-06-28
Product Code
DecisionSubstantially Equivalent

Device Summary

DENTAL CASSETTE HOLDERS is the device name listed in this FDA 510(k) record. The listed applicant is Xre Corp.. It received FDA 510(k) clearance on 1983-06-28 under 510(k) number K837515. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL CASSETTE HOLDERS?

DENTAL CASSETTE HOLDERS is a medical device that received FDA 510(k) clearance on 1983-06-28. The listed applicant is Xre Corp.. The 510(k) number is K837515.

When did DENTAL CASSETTE HOLDERS receive FDA 510(k) clearance?

DENTAL CASSETTE HOLDERS received FDA 510(k) clearance on 1983-06-28, under 510(k) number K837515.

Who is the listed applicant for DENTAL CASSETTE HOLDERS?

The FDA 510(k) record lists Xre Corp. 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 Xre 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.

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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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