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FDA 510(k)

STORZ DIAGNOSTIC MICROSCOPE SYSTEM

K-Number: K882269 · 1988-06-23

Decision Date1988-06-23
Product CodeEPT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STORZ DIAGNOSTIC MICROSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1988-06-23 under 510(k) number K882269. The device is classified under product code EPT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ DIAGNOSTIC MICROSCOPE SYSTEM?

STORZ DIAGNOSTIC MICROSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is Storz Instrument Co.. The 510(k) number is K882269.

When did STORZ DIAGNOSTIC MICROSCOPE SYSTEM receive FDA 510(k) clearance?

STORZ DIAGNOSTIC MICROSCOPE SYSTEM received FDA 510(k) clearance on 1988-06-23, under 510(k) number K882269.

Who is the listed applicant for STORZ DIAGNOSTIC MICROSCOPE SYSTEM?

The FDA 510(k) record lists Storz Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STORZ DIAGNOSTIC MICROSCOPE SYSTEM?

The FDA product code for STORZ DIAGNOSTIC MICROSCOPE SYSTEM is EPT.

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 Storz Instrument 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.

View all 101 devices →

Related Devices (Code: EPT)

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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