ITC MODEL ADOBE 100 CANAL
K-Number: K931591 · 1993-05-19
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Device Summary
Frequently Asked Questions
What is the ITC MODEL ADOBE 100 CANAL?
ITC MODEL ADOBE 100 CANAL is a medical device that received FDA 510(k) clearance on 1993-05-19. The listed applicant is Widex Hearing Aid Co., Inc.. The 510(k) number is K931591.
When did ITC MODEL ADOBE 100 CANAL receive FDA 510(k) clearance?
ITC MODEL ADOBE 100 CANAL received FDA 510(k) clearance on 1993-05-19, under 510(k) number K931591.
Who is the listed applicant for ITC MODEL ADOBE 100 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 ITC MODEL ADOBE 100 CANAL?
The FDA product code for ITC MODEL ADOBE 100 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.
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