WIDEX SENSO DIGITAL (MINI CANAL)
K-Number: K971535 · 1997-06-06
Advertisement
Device Summary
Frequently Asked Questions
What is the WIDEX SENSO DIGITAL (MINI CANAL)?
WIDEX SENSO DIGITAL (MINI CANAL) is a medical device that received FDA 510(k) clearance on 1997-06-06. The listed applicant is Widex Hearing Aid Co., Inc.. The 510(k) number is K971535.
When did WIDEX SENSO DIGITAL (MINI CANAL) receive FDA 510(k) clearance?
WIDEX SENSO DIGITAL (MINI CANAL) received FDA 510(k) clearance on 1997-06-06, under 510(k) number K971535.
Who is the listed applicant for WIDEX SENSO DIGITAL (MINI CANAL)?
The FDA 510(k) record lists Widex Hearing Aid Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WIDEX SENSO DIGITAL (MINI CANAL)?
The FDA product code for WIDEX SENSO DIGITAL (MINI CANAL) 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 Widex Hearing Aid Co., 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.
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