PHONAK 9900 CIC
K-Number: K953921 · 1995-09-18
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Device Summary
Frequently Asked Questions
What is the PHONAK 9900 CIC?
PHONAK 9900 CIC is a medical device that received FDA 510(k) clearance on 1995-09-18. The listed applicant is Phonak, Inc.. The 510(k) number is K953921.
When did PHONAK 9900 CIC receive FDA 510(k) clearance?
PHONAK 9900 CIC received FDA 510(k) clearance on 1995-09-18, under 510(k) number K953921.
Who is the listed applicant for PHONAK 9900 CIC?
The FDA 510(k) record lists Phonak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHONAK 9900 CIC?
The FDA product code for PHONAK 9900 CIC 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 Phonak, 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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