PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTS
K-Number: K941734 · 1994-05-13
Advertisement
Device Summary
Frequently Asked Questions
What is the PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTS?
PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-05-13. The listed applicant is Phonak, Inc.. The 510(k) number is K941734.
When did PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTS receive FDA 510(k) clearance?
PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTS received FDA 510(k) clearance on 1994-05-13, under 510(k) number K941734.
Who is the listed applicant for PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTS?
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 SONO-FORTE 331X BTE HEARING INSTRUMENTS?
The FDA product code for PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTS 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.
Advertisement