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FDA 510(k)

KSEA BIPOLAR COAGULATING ELECTRODES

K-Number: K001630 · 2000-07-19

ApplicantKarl Storz Endoscopy
Decision Date2000-07-19
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

KSEA BIPOLAR COAGULATING ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy. It received FDA 510(k) clearance on 2000-07-19 under 510(k) number K001630. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KSEA BIPOLAR COAGULATING ELECTRODES?

KSEA BIPOLAR COAGULATING ELECTRODES is a medical device that received FDA 510(k) clearance on 2000-07-19. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K001630.

When did KSEA BIPOLAR COAGULATING ELECTRODES receive FDA 510(k) clearance?

KSEA BIPOLAR COAGULATING ELECTRODES received FDA 510(k) clearance on 2000-07-19, under 510(k) number K001630.

Who is the listed applicant for KSEA BIPOLAR COAGULATING ELECTRODES?

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

What is the FDA product code for KSEA BIPOLAR COAGULATING ELECTRODES?

The FDA product code for KSEA BIPOLAR COAGULATING ELECTRODES is GWG.

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Other records listing Karl Storz Endoscopy 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: GWG)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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