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FDA 510(k)

ONE STEP MARIJUANA CARD TEST

K-Number: K970548 · 1997-07-03

Decision Date1997-07-03
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ONE STEP MARIJUANA CARD TEST is the device name listed in this FDA 510(k) record. The listed applicant is Teco Diagnostics. It received FDA 510(k) clearance on 1997-07-03 under 510(k) number K970548. 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 ONE STEP MARIJUANA CARD TEST?

ONE STEP MARIJUANA CARD TEST is a medical device that received FDA 510(k) clearance on 1997-07-03. The listed applicant is Teco Diagnostics. The 510(k) number is K970548.

When did ONE STEP MARIJUANA CARD TEST receive FDA 510(k) clearance?

ONE STEP MARIJUANA CARD TEST received FDA 510(k) clearance on 1997-07-03, under 510(k) number K970548.

Who is the listed applicant for ONE STEP MARIJUANA CARD TEST?

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

What is the FDA product code for ONE STEP MARIJUANA CARD TEST?

The FDA product code for ONE STEP MARIJUANA CARD TEST is LDJ.

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 Teco Diagnostics 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 49 devices →

Related Devices (Code: LDJ)

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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