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FDA 510(k)

EURION LOTOS P HEARING AID

K-Number: K921257 · 1992-05-15

ApplicantManro Corp.
Decision Date1992-05-15
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EURION LOTOS P HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Manro Corp.. It received FDA 510(k) clearance on 1992-05-15 under 510(k) number K921257. 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 EURION LOTOS P HEARING AID?

EURION LOTOS P HEARING AID is a medical device that received FDA 510(k) clearance on 1992-05-15. The listed applicant is Manro Corp.. The 510(k) number is K921257.

When did EURION LOTOS P HEARING AID receive FDA 510(k) clearance?

EURION LOTOS P HEARING AID received FDA 510(k) clearance on 1992-05-15, under 510(k) number K921257.

Who is the listed applicant for EURION LOTOS P HEARING AID?

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

What is the FDA product code for EURION LOTOS P HEARING AID?

The FDA product code for EURION LOTOS P HEARING AID is ESD.

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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.

K232999Lyric4 Hearing AidSonova AGK130790LYRIC2Phonak, LLCK081136LYRIC HEARING AIDInsound Medical, Inc.K021867INSOUND XT SERIES HEARING AIDInsound Medical, Inc.K003558TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)Siemens Hearing Instruments, Inc.K984518SONIC INNOVATIONS COMPLETELY-IN-THE-CANAL DSP HEARING AID WITH SOFT SHELLSonic Innovations, Inc.

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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