Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ABUSCREEN (R) EIA CANNABINOIDS

K-Number: K870377 · 1987-03-16

Decision Date1987-03-16
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ABUSCREEN (R) EIA CANNABINOIDS is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1987-03-16 under 510(k) number K870377. 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 ABUSCREEN (R) EIA CANNABINOIDS?

ABUSCREEN (R) EIA CANNABINOIDS is a medical device that received FDA 510(k) clearance on 1987-03-16. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K870377.

When did ABUSCREEN (R) EIA CANNABINOIDS receive FDA 510(k) clearance?

ABUSCREEN (R) EIA CANNABINOIDS received FDA 510(k) clearance on 1987-03-16, under 510(k) number K870377.

Who is the listed applicant for ABUSCREEN (R) EIA CANNABINOIDS?

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 (R) EIA CANNABINOIDS?

The FDA product code for ABUSCREEN (R) EIA CANNABINOIDS 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 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.

View all 296 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.

↑