Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER

K-Number: K882409 · 1988-07-05

Decision Date1988-07-05
Product CodeEPF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER is the device name listed in this FDA 510(k) record. The listed applicant is Phonic Ear, Inc.. It received FDA 510(k) clearance on 1988-07-05 under 510(k) number K882409. The device is classified under product code EPF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER?

PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER is a medical device that received FDA 510(k) clearance on 1988-07-05. The listed applicant is Phonic Ear, Inc.. The 510(k) number is K882409.

When did PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER receive FDA 510(k) clearance?

PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER received FDA 510(k) clearance on 1988-07-05, under 510(k) number K882409.

Who is the listed applicant for PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER?

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

What is the FDA product code for PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER?

The FDA product code for PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER is EPF.

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 Phonic Ear, 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 31 devices →

Related Devices (Code: EPF)

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.

↑