Karl Storz Xenon 300 Light Source for Non-Flash Applications

by Karl Storz Endoscopy-America, Inc. 510(k)

Active United States

510(k) K962595

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK962595	Date4 Sep 1996Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 8 Oct 2026.

Specification

510(k)

510(k) Number: K962595
FDA Product Code: FFS

Device Class: Class II
Regulation: 21 CFR Part 876.1500
Advisory Committee: Gastroenterology, Urology
FDA Decision: SESE Substantially Equivalent

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