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FDA 510(k)

POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &

K-Number: K850186 · 1985-03-27

ApplicantRobert Bosch Corp.
Decision Date1985-03-27
Product Code
DecisionSubstantially Equivalent

Device Summary

POST AURICULAR HEARING AIDS STAR 33PP, 44,55F & 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 1985-03-27 under 510(k) number K850186. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &?

POST AURICULAR HEARING AIDS STAR 33PP, 44,55F & is a medical device that received FDA 510(k) clearance on 1985-03-27. The listed applicant is Robert Bosch Corp.. The 510(k) number is K850186.

When did POST AURICULAR HEARING AIDS STAR 33PP, 44,55F & receive FDA 510(k) clearance?

POST AURICULAR HEARING AIDS STAR 33PP, 44,55F & received FDA 510(k) clearance on 1985-03-27, under 510(k) number K850186.

Who is the listed applicant for POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &?

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

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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.

K854492ERG 551 ERGOMETER, BICYCLEK854493ERG 555 COUCH ERGOMETERK854491ERG 550 ERGOMETER BICYCLEK853541SP 4K853154HV-4K853271HEARING AID ANALYSIS SYSTEM

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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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