Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

IN THE CANAL AID OTOSONIC ACS II WITH SRR

K-Number: K931881 · 1993-07-02

Decision Date1993-07-02
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

IN THE CANAL AID OTOSONIC ACS II WITH SRR is the device name listed in this FDA 510(k) record. The listed applicant is Beltone Electronics Corp.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K931881. 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 IN THE CANAL AID OTOSONIC ACS II WITH SRR?

IN THE CANAL AID OTOSONIC ACS II WITH SRR is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Beltone Electronics Corp.. The 510(k) number is K931881.

When did IN THE CANAL AID OTOSONIC ACS II WITH SRR receive FDA 510(k) clearance?

IN THE CANAL AID OTOSONIC ACS II WITH SRR received FDA 510(k) clearance on 1993-07-02, under 510(k) number K931881.

Who is the listed applicant for IN THE CANAL AID OTOSONIC ACS II WITH SRR?

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

What is the FDA product code for IN THE CANAL AID OTOSONIC ACS II WITH SRR?

The FDA product code for IN THE CANAL AID OTOSONIC ACS II WITH SRR 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 Beltone Electronics 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 42 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑