BTE HEARING AID SIEMENS MODEL 284PP-ASP
K-Number: K884583 · 1989-01-18
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Device Summary
Frequently Asked Questions
What is the BTE HEARING AID SIEMENS MODEL 284PP-ASP?
BTE HEARING AID SIEMENS MODEL 284PP-ASP is a medical device that received FDA 510(k) clearance on 1989-01-18. The listed applicant is Siemens Hearing Instruments, Inc.. The 510(k) number is K884583.
When did BTE HEARING AID SIEMENS MODEL 284PP-ASP receive FDA 510(k) clearance?
BTE HEARING AID SIEMENS MODEL 284PP-ASP received FDA 510(k) clearance on 1989-01-18, under 510(k) number K884583.
Who is the listed applicant for BTE HEARING AID SIEMENS MODEL 284PP-ASP?
The FDA 510(k) record lists Siemens Hearing Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BTE HEARING AID SIEMENS MODEL 284PP-ASP?
The FDA product code for BTE HEARING AID SIEMENS MODEL 284PP-ASP 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 Siemens Hearing Instruments, 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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