BTE PICO SCD, PICO SC
K-Number: K900831 · 1990-05-23
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Device Summary
Frequently Asked Questions
What is the BTE PICO SCD, PICO SC?
BTE PICO SCD, PICO SC is a medical device that received FDA 510(k) clearance on 1990-05-23. The listed applicant is Phonak, Inc.. The 510(k) number is K900831.
When did BTE PICO SCD, PICO SC receive FDA 510(k) clearance?
BTE PICO SCD, PICO SC received FDA 510(k) clearance on 1990-05-23, under 510(k) number K900831.
Who is the listed applicant for BTE PICO SCD, PICO SC?
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 BTE PICO SCD, PICO SC?
The FDA product code for BTE PICO SCD, PICO SC is ESD.
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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