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FDA 510(k)

KARL STORZ KNIVES, CURETTES

K-Number: K945686 · 1995-02-13

Decision Date1995-02-13
Product CodeEZO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ KNIVES, CURETTES is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1995-02-13 under 510(k) number K945686. The device is classified under product code EZO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ KNIVES, CURETTES?

KARL STORZ KNIVES, CURETTES is a medical device that received FDA 510(k) clearance on 1995-02-13. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K945686.

When did KARL STORZ KNIVES, CURETTES receive FDA 510(k) clearance?

KARL STORZ KNIVES, CURETTES received FDA 510(k) clearance on 1995-02-13, under 510(k) number K945686.

Who is the listed applicant for KARL STORZ KNIVES, CURETTES?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KARL STORZ KNIVES, CURETTES?

The FDA product code for KARL STORZ KNIVES, CURETTES is EZO.

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 KARL STORZ Endoscopy-America, Inc. 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 355 devices →

Related Devices (Code: EZO)

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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