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FDA 510(k)

BOSCH HEARING INSTRUMENTS

K-Number: K812503 · 1981-09-24

ApplicantRetlif, Inc.
Decision Date1981-09-24
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BOSCH HEARING INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Retlif, Inc.. It received FDA 510(k) clearance on 1981-09-24 under 510(k) number K812503. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOSCH HEARING INSTRUMENTS?

BOSCH HEARING INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1981-09-24. The listed applicant is Retlif, Inc.. The 510(k) number is K812503.

When did BOSCH HEARING INSTRUMENTS receive FDA 510(k) clearance?

BOSCH HEARING INSTRUMENTS received FDA 510(k) clearance on 1981-09-24, under 510(k) number K812503.

Who is the listed applicant for BOSCH HEARING INSTRUMENTS?

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

What is the FDA product code for BOSCH HEARING INSTRUMENTS?

The FDA product code for BOSCH HEARING INSTRUMENTS is CCQ.

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.

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Other records listing Retlif, 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.

K800904TONOTEST BLOOD PRESSURE MONITOR

Related Devices (Code: CCQ)

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.

K972397EZ SPRAYIntertex Research, Inc.K964956E-Z SPACER MASK (SMALL)Airpharma, LLCK961894MDI TUTORMdi Tutor, Inc.K961455MEDSHIELD/AEROCHAMBERDiemolding Corp.K960593SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-100Aradigm Corp.K922033SALINE SOLUTION- STERILETrinity Laboratories, 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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