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FDA 510(k)

BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4

K-Number: K900830 · 1990-05-23

ApplicantPhonak, Inc.
Decision Date1990-05-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4 is the device name listed in this FDA 510(k) record. The listed applicant is Phonak, Inc.. It received FDA 510(k) clearance on 1990-05-23 under 510(k) number K900830. 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 BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4?

BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4 is a medical device that received FDA 510(k) clearance on 1990-05-23. The listed applicant is Phonak, Inc.. The 510(k) number is K900830.

When did BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4 receive FDA 510(k) clearance?

BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4 received FDA 510(k) clearance on 1990-05-23, under 510(k) number K900830.

Who is the listed applicant for BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4?

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

What is the FDA product code for BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4?

The FDA product code for BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4 is ESD.

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Other records listing Phonak, Inc. as applicant

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Related Devices (Code: ESD)

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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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