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)

VOROBA PROGRAMMABLE AUDITORY COMPARATOR

K-Number: K860171 · 1986-05-02

Decision Date1986-05-02
Product CodeKHL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VOROBA PROGRAMMABLE AUDITORY COMPARATOR is the device name listed in this FDA 510(k) record. The listed applicant is Voroba Technologies Assoc.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K860171. The device is classified under product code KHL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOROBA PROGRAMMABLE AUDITORY COMPARATOR?

VOROBA PROGRAMMABLE AUDITORY COMPARATOR is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Voroba Technologies Assoc.. The 510(k) number is K860171.

When did VOROBA PROGRAMMABLE AUDITORY COMPARATOR receive FDA 510(k) clearance?

VOROBA PROGRAMMABLE AUDITORY COMPARATOR received FDA 510(k) clearance on 1986-05-02, under 510(k) number K860171.

Who is the listed applicant for VOROBA PROGRAMMABLE AUDITORY COMPARATOR?

The FDA 510(k) record lists Voroba Technologies Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOROBA PROGRAMMABLE AUDITORY COMPARATOR?

The FDA product code for VOROBA PROGRAMMABLE AUDITORY COMPARATOR is KHL.

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 Voroba Technologies Assoc. 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.

Related Devices (Code: KHL)

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.

↑