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FDA 510(k)

TARGET READER

K-Number: K885254 · 1989-01-27

ApplicantV-Tech, Inc.
Decision Date1989-01-27
Product CodeJQT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TARGET READER 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 1989-01-27 under 510(k) number K885254. The device is classified under product code JQT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TARGET READER?

TARGET READER is a medical device that received FDA 510(k) clearance on 1989-01-27. The listed applicant is V-Tech, Inc.. The 510(k) number is K885254.

When did TARGET READER receive FDA 510(k) clearance?

TARGET READER received FDA 510(k) clearance on 1989-01-27, under 510(k) number K885254.

Who is the listed applicant for TARGET READER?

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 READER?

The FDA product code for TARGET READER is JQT.

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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.

K914303TARGET(TM)-HOGK910893TARGET(TM) CANNABINOIDS-R TESTK910892TARGET(TM) CANNABINOIDS-V TESTK910739TARGET AMPHETAMINE/METHAMPHETAMINE-R (READER METH)K910738TARGET AMPHETAMINE/METHAMPHETAMINE-V (VISUAL METH)K910123TARGET COCAINE METABOLITE-V

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Related Devices (Code: JQT)

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.

K111356ASIMANAGER - ATArlington Scientific, Inc.K944185ISOSCANIsolab, Inc.K915332MODEL 795 FLUOROMETER/DENSITOMETERCiba Corning Diagnostics Corp.K860645ELECTROPHORESIS DATA CENTER (EDC)Helena LaboratoriesK862956ICON READERHybritech, Inc.K853734APOLLO DENSITOMETERAstral Medical Systems

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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