TARGET(TM)-HOG
K-Number: K914303 · 1991-10-11
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Device Summary
Frequently Asked Questions
What is the TARGET(TM)-HOG?
TARGET(TM)-HOG is a medical device that received FDA 510(k) clearance on 1991-10-11. The listed applicant is V-Tech, Inc.. The 510(k) number is K914303.
When did TARGET(TM)-HOG receive FDA 510(k) clearance?
TARGET(TM)-HOG received FDA 510(k) clearance on 1991-10-11, under 510(k) number K914303.
Who is the listed applicant for TARGET(TM)-HOG?
The FDA 510(k) record lists V-Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TARGET(TM)-HOG?
The FDA product code for TARGET(TM)-HOG is JHI.
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 V-Tech, 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.
Related Devices (Code: JHI)
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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