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FDA 510(k)

TARGET(TM) HOG ONE STEP

K-Number: K903937 · 1990-10-22

ApplicantV-Tech, Inc.
Decision Date1990-10-22
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TARGET(TM) HOG ONE STEP is the device name listed in this FDA 510(k) record. The listed applicant is V-Tech, Inc.. It received FDA 510(k) clearance on 1990-10-22 under 510(k) number K903937. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TARGET(TM) HOG ONE STEP?

TARGET(TM) HOG ONE STEP is a medical device that received FDA 510(k) clearance on 1990-10-22. The listed applicant is V-Tech, Inc.. The 510(k) number is K903937.

When did TARGET(TM) HOG ONE STEP receive FDA 510(k) clearance?

TARGET(TM) HOG ONE STEP received FDA 510(k) clearance on 1990-10-22, under 510(k) number K903937.

Who is the listed applicant for TARGET(TM) HOG ONE STEP?

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 ONE STEP?

The FDA product code for TARGET(TM) HOG ONE STEP 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.

View all 22 devices →

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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