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FDA 510(k)

ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100

K-Number: K961620 · 1996-06-13

Decision Date1996-06-13
Product CodeLAT
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100 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 1996-06-13 under 510(k) number K961620. The device is classified under product code LAT. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100?

ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100 is a medical device that received FDA 510(k) clearance on 1996-06-13. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K961620.

When did ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100 receive FDA 510(k) clearance?

ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100 received FDA 510(k) clearance on 1996-06-13, under 510(k) number K961620.

Who is the listed applicant for ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100?

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 ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100?

The FDA product code for ABISCREEN ONLINE FOR CANNABINOIDS - ES 50/100 is LAT.

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: LAT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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