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FDA 510(k)

DZIDRA GLASS FOR USE IN OPHTHALMOLOGY

K-Number: K864656 · 1987-02-25

Decision Date1987-02-25
Product Code
DecisionSubstantially Equivalent

Device Summary

DZIDRA GLASS FOR USE IN OPHTHALMOLOGY 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 K864656. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DZIDRA GLASS FOR USE IN OPHTHALMOLOGY?

DZIDRA GLASS FOR USE IN OPHTHALMOLOGY 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 K864656.

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

DZIDRA GLASS FOR USE IN OPHTHALMOLOGY received FDA 510(k) clearance on 1987-02-25, under 510(k) number K864656.

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

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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