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FDA 510(k)

VOCALTECH VOCAL FEEDBACK DEVICE

K-Number: K871590 · 1987-10-06

Decision Date1987-10-06
Product CodeKTH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VOCALTECH VOCAL FEEDBACK DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Vocaltech C/O Hogan & Hartson. It received FDA 510(k) clearance on 1987-10-06 under 510(k) number K871590. The device is classified under product code KTH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOCALTECH VOCAL FEEDBACK DEVICE?

VOCALTECH VOCAL FEEDBACK DEVICE is a medical device that received FDA 510(k) clearance on 1987-10-06. The listed applicant is Vocaltech C/O Hogan & Hartson. The 510(k) number is K871590.

When did VOCALTECH VOCAL FEEDBACK DEVICE receive FDA 510(k) clearance?

VOCALTECH VOCAL FEEDBACK DEVICE received FDA 510(k) clearance on 1987-10-06, under 510(k) number K871590.

Who is the listed applicant for VOCALTECH VOCAL FEEDBACK DEVICE?

The FDA 510(k) record lists Vocaltech C/O Hogan & Hartson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOCALTECH VOCAL FEEDBACK DEVICE?

The FDA product code for VOCALTECH VOCAL FEEDBACK DEVICE is KTH.

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.

Related Devices (Code: KTH)

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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