CRESTLINE CL IN-THE-EAR HEARING AID
K-Number: K850980 · 1985-06-19
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Device Summary
Frequently Asked Questions
What is the CRESTLINE CL IN-THE-EAR HEARING AID?
CRESTLINE CL IN-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1985-06-19. The listed applicant is Dahlberg Electronics, Inc.. The 510(k) number is K850980.
When did CRESTLINE CL IN-THE-EAR HEARING AID receive FDA 510(k) clearance?
CRESTLINE CL IN-THE-EAR HEARING AID received FDA 510(k) clearance on 1985-06-19, under 510(k) number K850980.
Who is the listed applicant for CRESTLINE CL IN-THE-EAR HEARING AID?
The FDA 510(k) record lists Dahlberg Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRESTLINE CL IN-THE-EAR HEARING AID?
The FDA product code for CRESTLINE CL 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 Dahlberg Electronics, 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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