VOROBA PROGRAMMABLE AUDITORY COMPARATOR
K-Number: K860171 · 1986-05-02
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Device Summary
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.
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