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FDA 510(k)

ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE

K-Number: K012595 · 2001-10-15

ApplicantACON Laboratories, Inc.
Decision Date2001-10-15
Product CodeDJR
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is ACON Laboratories, Inc.. It received FDA 510(k) clearance on 2001-10-15 under 510(k) number K012595. The device is classified under product code DJR. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE?

ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE is a medical device that received FDA 510(k) clearance on 2001-10-15. The listed applicant is ACON Laboratories, Inc.. The 510(k) number is K012595.

When did ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE receive FDA 510(k) clearance?

ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE received FDA 510(k) clearance on 2001-10-15, under 510(k) number K012595.

Who is the listed applicant for ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE?

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

What is the FDA product code for ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE?

The FDA product code for ACON MTD ONE STEP METHADONE TEST STRIP AND TEST DEVICE is DJR.

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Related Devices (Code: DJR)

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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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