PHONAK PICO-FORTE SC-2
K-Number: K932734 · 1993-07-27
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Device Summary
Frequently Asked Questions
What is the PHONAK PICO-FORTE SC-2?
PHONAK PICO-FORTE SC-2 is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Phonak, Inc.. The 510(k) number is K932734.
When did PHONAK PICO-FORTE SC-2 receive FDA 510(k) clearance?
PHONAK PICO-FORTE SC-2 received FDA 510(k) clearance on 1993-07-27, under 510(k) number K932734.
Who is the listed applicant for PHONAK PICO-FORTE SC-2?
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 PICO-FORTE SC-2?
The FDA product code for PHONAK PICO-FORTE SC-2 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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