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FDA 510(k)

PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II

K-Number: K893432 · 1989-08-04

Decision Date1989-08-04
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II is the device name listed in this FDA 510(k) record. The listed applicant is Electone, Inc.. It received FDA 510(k) clearance on 1989-08-04 under 510(k) number K893432. 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 PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II?

PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II is a medical device that received FDA 510(k) clearance on 1989-08-04. The listed applicant is Electone, Inc.. The 510(k) number is K893432.

When did PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II receive FDA 510(k) clearance?

PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II received FDA 510(k) clearance on 1989-08-04, under 510(k) number K893432.

Who is the listed applicant for PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II?

The FDA 510(k) record lists Electone, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II?

The FDA product code for PERSONAL AMPLIFIER RECHARGEABLE MODEL TRIUMPH II 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 Electone, 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.

View all 73 devices →

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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