CUSTOM ITE HEARING AID MODELS C AND M
K-Number: K902351 · 1990-06-14
Advertisement
Device Summary
Frequently Asked Questions
What is the CUSTOM ITE HEARING AID MODELS C AND M?
CUSTOM ITE HEARING AID MODELS C AND M is a medical device that received FDA 510(k) clearance on 1990-06-14. The listed applicant is Oticon Corp.. The 510(k) number is K902351.
When did CUSTOM ITE HEARING AID MODELS C AND M receive FDA 510(k) clearance?
CUSTOM ITE HEARING AID MODELS C AND M received FDA 510(k) clearance on 1990-06-14, under 510(k) number K902351.
Who is the listed applicant for CUSTOM ITE HEARING AID MODELS C AND M?
The FDA 510(k) record lists Oticon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUSTOM ITE HEARING AID MODELS C AND M?
The FDA product code for CUSTOM ITE HEARING AID MODELS C AND M is ESD.
Related Clinical Trials
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.
Other records listing Oticon Corp. 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: ESD)
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.
Advertisement