METHADONE
K-Number: K013001 · 2002-03-20
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Device Summary
Frequently Asked Questions
What is the METHADONE?
METHADONE is a medical device that received FDA 510(k) clearance on 2002-03-20. The listed applicant is Abbott Laboratories. The 510(k) number is K013001.
When did METHADONE receive FDA 510(k) clearance?
METHADONE received FDA 510(k) clearance on 2002-03-20, under 510(k) number K013001.
Who is the listed applicant for METHADONE?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for METHADONE?
The FDA product code for METHADONE is DJR.
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 Abbott Laboratories 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.
Related Devices (Code: DJR)
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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