SIEMENS 10A FACEPLATE WITH CIC INSTRUMENTS
K-Number: K943380 · 1995-01-05
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Device Summary
Frequently Asked Questions
What is the SIEMENS 10A FACEPLATE WITH CIC INSTRUMENTS?
SIEMENS 10A FACEPLATE WITH CIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1995-01-05. The listed applicant is Siemens Hearing Instruments, Inc.. The 510(k) number is K943380.
When did SIEMENS 10A FACEPLATE WITH CIC INSTRUMENTS receive FDA 510(k) clearance?
SIEMENS 10A FACEPLATE WITH CIC INSTRUMENTS received FDA 510(k) clearance on 1995-01-05, under 510(k) number K943380.
Who is the listed applicant for SIEMENS 10A FACEPLATE WITH CIC INSTRUMENTS?
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 SIEMENS 10A FACEPLATE WITH CIC INSTRUMENTS?
The FDA product code for SIEMENS 10A FACEPLATE WITH CIC 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 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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