FDA 510(k)

KSEA PERCUTANEOUS FORAMINOSCOPY SET

K-Number: K001918 · 2000-09-19

ApplicantKARL STORZ Endoscopy-America, Inc.

Decision Date2000-09-19

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

KSEA PERCUTANEOUS FORAMINOSCOPY SET 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 2000-09-19 under 510(k) number K001918. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KSEA PERCUTANEOUS FORAMINOSCOPY SET?

KSEA PERCUTANEOUS FORAMINOSCOPY SET is a medical device that received FDA 510(k) clearance on 2000-09-19. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K001918.

When did KSEA PERCUTANEOUS FORAMINOSCOPY SET receive FDA 510(k) clearance?

KSEA PERCUTANEOUS FORAMINOSCOPY SET received FDA 510(k) clearance on 2000-09-19, under 510(k) number K001918.

Who is the listed applicant for KSEA PERCUTANEOUS FORAMINOSCOPY SET?

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 KSEA PERCUTANEOUS FORAMINOSCOPY SET?

The FDA product code for KSEA PERCUTANEOUS FORAMINOSCOPY SET is HRX.

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Other records listing KARL STORZ Endoscopy-America, Inc. as applicant

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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.