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FDA 510(k)

MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM

K-Number: K903760 · 1990-10-05

Decision Date1990-10-05
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Hearing Instruments, Inc.. It received FDA 510(k) clearance on 1990-10-05 under 510(k) number K903760. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM?

MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM is a medical device that received FDA 510(k) clearance on 1990-10-05. The listed applicant is Siemens Hearing Instruments, Inc.. The 510(k) number is K903760.

When did MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM receive FDA 510(k) clearance?

MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM received FDA 510(k) clearance on 1990-10-05, under 510(k) number K903760.

Who is the listed applicant for MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM?

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 MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM?

The FDA product code for MODEL TRITON 3000 BTE HEARING AID AND PMC SYSTEM 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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