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FDA 510(k)

COCAINE DIPSTICK TEST, MODEL D747-A

K-Number: K010239 · 2001-06-25

ApplicantTeco Diagnostics
Decision Date2001-06-25
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

COCAINE DIPSTICK TEST, MODEL D747-A is the device name listed in this FDA 510(k) record. The listed applicant is Teco Diagnostics. It received FDA 510(k) clearance on 2001-06-25 under 510(k) number K010239. The device is classified under product code DIO. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COCAINE DIPSTICK TEST, MODEL D747-A?

COCAINE DIPSTICK TEST, MODEL D747-A is a medical device that received FDA 510(k) clearance on 2001-06-25. The listed applicant is Teco Diagnostics. The 510(k) number is K010239.

When did COCAINE DIPSTICK TEST, MODEL D747-A receive FDA 510(k) clearance?

COCAINE DIPSTICK TEST, MODEL D747-A received FDA 510(k) clearance on 2001-06-25, under 510(k) number K010239.

Who is the listed applicant for COCAINE DIPSTICK TEST, MODEL D747-A?

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 COCAINE DIPSTICK TEST, MODEL D747-A?

The FDA product code for COCAINE DIPSTICK TEST, MODEL D747-A is DIO.

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Related Devices (Code: DIO)

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.

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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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