DZIDRA GLASS FOR USE IN GENERAL MEDICAL
K-Number: K864679 · 1987-02-25
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Device Summary
Frequently Asked Questions
What is the DZIDRA GLASS FOR USE IN GENERAL MEDICAL?
DZIDRA GLASS FOR USE IN GENERAL MEDICAL 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 K864679.
When did DZIDRA GLASS FOR USE IN GENERAL MEDICAL receive FDA 510(k) clearance?
DZIDRA GLASS FOR USE IN GENERAL MEDICAL received FDA 510(k) clearance on 1987-02-25, under 510(k) number K864679.
Who is the listed applicant for DZIDRA GLASS FOR USE IN GENERAL MEDICAL?
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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