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FDA 510(k)

MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID

K-Number: K933291 · 1993-08-23

Decision Date1993-08-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Maico Hearing Instruments, Inc.. It received FDA 510(k) clearance on 1993-08-23 under 510(k) number K933291. 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 MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID?

MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID is a medical device that received FDA 510(k) clearance on 1993-08-23. The listed applicant is Maico Hearing Instruments, Inc.. The 510(k) number is K933291.

When did MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID receive FDA 510(k) clearance?

MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID received FDA 510(k) clearance on 1993-08-23, under 510(k) number K933291.

Who is the listed applicant for MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID?

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

What is the FDA product code for MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID?

The FDA product code for MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID 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 Maico Hearing Instruments, 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 58 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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