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FDA 510(k)

STORZ SUPER SORB MICRO EYE SPONGE

K-Number: K800082 · 1980-02-05

Decision Date1980-02-05
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

STORZ SUPER SORB MICRO EYE SPONGE 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 1980-02-05 under 510(k) number K800082. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ SUPER SORB MICRO EYE SPONGE?

STORZ SUPER SORB MICRO EYE SPONGE is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Storz Instrument Co.. The 510(k) number is K800082.

When did STORZ SUPER SORB MICRO EYE SPONGE receive FDA 510(k) clearance?

STORZ SUPER SORB MICRO EYE SPONGE received FDA 510(k) clearance on 1980-02-05, under 510(k) number K800082.

Who is the listed applicant for STORZ SUPER SORB MICRO EYE SPONGE?

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 SUPER SORB MICRO EYE SPONGE?

The FDA product code for STORZ SUPER SORB MICRO EYE SPONGE is EFQ.

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: EFQ)

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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