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FDA 510(k)

DZIDRA GLASS FOR USE IN NEUROLOGY

K-Number: K864678 · 1987-02-25

Decision Date1987-02-25
Product Code
DecisionSubstantially Equivalent

Device Summary

DZIDRA GLASS FOR USE IN NEUROLOGY is the device name listed in this FDA 510(k) record. The listed applicant is Glen Whitten, Dds. It received FDA 510(k) clearance on 1987-02-25 under 510(k) number K864678. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DZIDRA GLASS FOR USE IN NEUROLOGY?

DZIDRA GLASS FOR USE IN NEUROLOGY is a medical device that received FDA 510(k) clearance on 1987-02-25. The listed applicant is Glen Whitten, Dds. The 510(k) number is K864678.

When did DZIDRA GLASS FOR USE IN NEUROLOGY receive FDA 510(k) clearance?

DZIDRA GLASS FOR USE IN NEUROLOGY received FDA 510(k) clearance on 1987-02-25, under 510(k) number K864678.

Who is the listed applicant for DZIDRA GLASS FOR USE IN NEUROLOGY?

The FDA 510(k) record lists Glen Whitten, Dds 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 Glen Whitten, Dds 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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