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FDA 510(k)

STC CANNABINOIDS MICRO-PLATE EIA

K-Number: K973750 · 1998-02-13

Decision Date1998-02-13
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

STC CANNABINOIDS MICRO-PLATE EIA is the device name listed in this FDA 510(k) record. The listed applicant is OraSure Technologies, Inc.. It received FDA 510(k) clearance on 1998-02-13 under 510(k) number K973750. 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 STC CANNABINOIDS MICRO-PLATE EIA?

STC CANNABINOIDS MICRO-PLATE EIA is a medical device that received FDA 510(k) clearance on 1998-02-13. The listed applicant is OraSure Technologies, Inc.. The 510(k) number is K973750.

When did STC CANNABINOIDS MICRO-PLATE EIA receive FDA 510(k) clearance?

STC CANNABINOIDS MICRO-PLATE EIA received FDA 510(k) clearance on 1998-02-13, under 510(k) number K973750.

Who is the listed applicant for STC CANNABINOIDS MICRO-PLATE EIA?

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

What is the FDA product code for STC CANNABINOIDS MICRO-PLATE EIA?

The FDA product code for STC CANNABINOIDS MICRO-PLATE EIA 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 OraSure Technologies, 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 29 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

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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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