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FDA 510(k)

DBEST TETRAHYDROCANNABINOL TEST KIT

K-Number: K983188 · 1998-11-18

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

Device Summary

DBEST TETRAHYDROCANNABINOL 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 K983188. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DBEST TETRAHYDROCANNABINOL TEST KIT?

DBEST TETRAHYDROCANNABINOL 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 K983188.

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

DBEST TETRAHYDROCANNABINOL TEST KIT received FDA 510(k) clearance on 1998-11-18, under 510(k) number K983188.

Who is the listed applicant for DBEST TETRAHYDROCANNABINOL 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 TETRAHYDROCANNABINOL TEST KIT?

The FDA product code for DBEST TETRAHYDROCANNABINOL TEST KIT is LDJ.

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Other records listing Ameritek, 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.

K001215DBEST HCG 2 IU/ML TEST KITK990873DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USEK990681DBSET MULTIDRUG SCREEN TEST KITK984269DBEST OCCULT BLOOD TEST KITK983191DBEST COCAINE TEST KITK983190DBEST OPIATES TEST KIT

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Related Devices (Code: LDJ)

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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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