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FDA 510(k)

DBEST METHAMPHETAMINES TEST KIT

K-Number: K983189 · 1998-11-18

ApplicantAmeritek, Inc.
Decision Date1998-11-18
Product CodeLAF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DBEST METHAMPHETAMINES TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ameritek, Inc.. It received FDA 510(k) clearance on 1998-11-18 under 510(k) number K983189. The device is classified under product code LAF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DBEST METHAMPHETAMINES TEST KIT?

DBEST METHAMPHETAMINES TEST KIT is a medical device that received FDA 510(k) clearance on 1998-11-18. The listed applicant is Ameritek, Inc.. The 510(k) number is K983189.

When did DBEST METHAMPHETAMINES TEST KIT receive FDA 510(k) clearance?

DBEST METHAMPHETAMINES TEST KIT received FDA 510(k) clearance on 1998-11-18, under 510(k) number K983189.

Who is the listed applicant for DBEST METHAMPHETAMINES TEST KIT?

The FDA 510(k) record lists Ameritek, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DBEST METHAMPHETAMINES TEST KIT?

The FDA product code for DBEST METHAMPHETAMINES TEST KIT is LAF.

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Other records listing Ameritek, Inc. as applicant

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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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