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FDA 510(k)

MICRO-PLATE COTININE EIA

K-Number: K974534 · 1998-05-18

Decision Date1998-05-18
Product CodeMKU
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MICRO-PLATE COTININE 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 1998-05-18 under 510(k) number K974534. The device is classified under product code MKU. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-PLATE COTININE EIA?

MICRO-PLATE COTININE EIA is a medical device that received FDA 510(k) clearance on 1998-05-18. The listed applicant is OraSure Technologies, Inc.. The 510(k) number is K974534.

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

MICRO-PLATE COTININE EIA received FDA 510(k) clearance on 1998-05-18, under 510(k) number K974534.

Who is the listed applicant for MICRO-PLATE COTININE 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 MICRO-PLATE COTININE EIA?

The FDA product code for MICRO-PLATE COTININE EIA is MKU.

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: MKU)

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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