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FDA 510(k)

KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522

K-Number: K080410 · 2008-04-09

Decision Date2008-04-09
Product CodeODA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522 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 2008-04-09 under 510(k) number K080410. The device is classified under product code ODA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522?

KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522 is a medical device that received FDA 510(k) clearance on 2008-04-09. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K080410.

When did KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522 receive FDA 510(k) clearance?

KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522 received FDA 510(k) clearance on 2008-04-09, under 510(k) number K080410.

Who is the listed applicant for KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522?

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 SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522?

The FDA product code for KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522 is ODA.

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.

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Related Devices (Code: ODA)

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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