PHILIPS 31 SERIES IN THE EAR HEARING AID
K-Number: K921463 · 1992-05-22
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Device Summary
Frequently Asked Questions
What is the PHILIPS 31 SERIES IN THE EAR HEARING AID?
PHILIPS 31 SERIES IN THE EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1992-05-22. The listed applicant is Philips Hearing Instruments Co.. The 510(k) number is K921463.
When did PHILIPS 31 SERIES IN THE EAR HEARING AID receive FDA 510(k) clearance?
PHILIPS 31 SERIES IN THE EAR HEARING AID received FDA 510(k) clearance on 1992-05-22, under 510(k) number K921463.
Who is the listed applicant for PHILIPS 31 SERIES IN THE EAR HEARING AID?
The FDA 510(k) record lists Philips Hearing Instruments Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHILIPS 31 SERIES IN THE EAR HEARING AID?
The FDA product code for PHILIPS 31 SERIES IN THE EAR HEARING AID 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 Philips Hearing Instruments Co. 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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