ABUSCREEN FP FOR MORPHINE
K-Number: K890888 · 1989-03-15
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Device Summary
Frequently Asked Questions
What is the ABUSCREEN FP FOR MORPHINE?
ABUSCREEN FP FOR MORPHINE is a medical device that received FDA 510(k) clearance on 1989-03-15. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K890888.
When did ABUSCREEN FP FOR MORPHINE receive FDA 510(k) clearance?
ABUSCREEN FP FOR MORPHINE received FDA 510(k) clearance on 1989-03-15, under 510(k) number K890888.
Who is the listed applicant for ABUSCREEN FP FOR MORPHINE?
The FDA 510(k) record lists Roche Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABUSCREEN FP FOR MORPHINE?
The FDA product code for ABUSCREEN FP FOR MORPHINE is DJG.
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 Roche Diagnostic Systems, 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.
Related Devices (Code: DJG)
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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