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FDA 510(k)

KARL STORZ Laryngoscopes and Accessories

K-Number: K252624 · 2026-05-15

Decision Date2026-05-15
Product CodeEQN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

KARL STORZ Laryngoscopes and Accessories 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 2026-05-15 under 510(k) number K252624. The device is classified under product code EQN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ Laryngoscopes and Accessories?

KARL STORZ Laryngoscopes and Accessories is a medical device that received FDA 510(k) clearance on 2026-05-15. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K252624.

When did KARL STORZ Laryngoscopes and Accessories receive FDA 510(k) clearance?

KARL STORZ Laryngoscopes and Accessories received FDA 510(k) clearance on 2026-05-15, under 510(k) number K252624.

Who is the listed applicant for KARL STORZ Laryngoscopes and Accessories?

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 Laryngoscopes and Accessories?

The FDA product code for KARL STORZ Laryngoscopes and Accessories is EQN.

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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Official Source

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