OTOPLAN
K-Number: K242120 · 2025-04-11
Device Summary
Frequently Asked Questions
What is the OTOPLAN?
OTOPLAN is a medical device that received FDA 510(k) clearance on 2025-04-11. The listed applicant is Cascination AG. The 510(k) number is K242120.
When did OTOPLAN receive FDA 510(k) clearance?
OTOPLAN received FDA 510(k) clearance on 2025-04-11, under 510(k) number K242120.
Who is the listed applicant for OTOPLAN?
The FDA 510(k) record lists Cascination AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OTOPLAN?
The FDA product code for OTOPLAN is QQE.
Other records listing Cascination AG 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.
Related Devices (Code: QQE)
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.
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.