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FDA 510(k)

BODY HEARING AIDS MT 80 SP

K-Number: K850185 · 1985-03-25

Decision Date1985-03-25
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BODY HEARING AIDS MT 80 SP is the device name listed in this FDA 510(k) record. The listed applicant is Robert Bosch Corp.. It received FDA 510(k) clearance on 1985-03-25 under 510(k) number K850185. 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 BODY HEARING AIDS MT 80 SP?

BODY HEARING AIDS MT 80 SP is a medical device that received FDA 510(k) clearance on 1985-03-25. The listed applicant is Robert Bosch Corp.. The 510(k) number is K850185.

When did BODY HEARING AIDS MT 80 SP receive FDA 510(k) clearance?

BODY HEARING AIDS MT 80 SP received FDA 510(k) clearance on 1985-03-25, under 510(k) number K850185.

Who is the listed applicant for BODY HEARING AIDS MT 80 SP?

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

What is the FDA product code for BODY HEARING AIDS MT 80 SP?

The FDA product code for BODY HEARING AIDS MT 80 SP 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 Robert Bosch Corp. 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 21 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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