Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KARL STORZ Laryngoscopes and Accessories

K-Number: K252624 · 2026-05-15

ApplicantKARL STORZ Endoscopy-America, Inc.
Decision Date2026-05-15
Product CodeEQN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

KARL STORZ Laryngoscopes and Accessories is a medical device manufactured by KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 2026-05-15 under approval 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. It is manufactured by KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K252624.

When was KARL STORZ Laryngoscopes and Accessories approved by the FDA?

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

What company makes KARL STORZ Laryngoscopes and Accessories?

KARL STORZ Laryngoscopes and Accessories is manufactured by KARL STORZ Endoscopy-America, Inc..

What is the FDA product code for KARL STORZ Laryngoscopes and Accessories?

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

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.

↑