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FDA 510(k)

BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K

K-Number: K951587 · 1995-06-30

ApplicantBeltone Electronics Corp.
Decision Date1995-06-30
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K is the device name listed in this FDA 510(k) record. The listed applicant is Beltone Electronics Corp.. It received FDA 510(k) clearance on 1995-06-30 under 510(k) number K951587. 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 BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K?

BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K is a medical device that received FDA 510(k) clearance on 1995-06-30. The listed applicant is Beltone Electronics Corp.. The 510(k) number is K951587.

When did BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K receive FDA 510(k) clearance?

BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K received FDA 510(k) clearance on 1995-06-30, under 510(k) number K951587.

Who is the listed applicant for BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K?

The FDA 510(k) record lists Beltone Electronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K?

The FDA product code for BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K is ESD.

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Other records listing Beltone Electronics Corp. as applicant

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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.

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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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