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FDA 510(k)

COAT-A-COUNT METHAMPHETAMIN #TKMA1

K-Number: K885071 · 1989-01-09

Decision Date1989-01-09
Product CodeLAF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

COAT-A-COUNT METHAMPHETAMIN #TKMA1 is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1989-01-09 under 510(k) number K885071. The device is classified under product code LAF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAT-A-COUNT METHAMPHETAMIN #TKMA1?

COAT-A-COUNT METHAMPHETAMIN #TKMA1 is a medical device that received FDA 510(k) clearance on 1989-01-09. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K885071.

When did COAT-A-COUNT METHAMPHETAMIN #TKMA1 receive FDA 510(k) clearance?

COAT-A-COUNT METHAMPHETAMIN #TKMA1 received FDA 510(k) clearance on 1989-01-09, under 510(k) number K885071.

Who is the listed applicant for COAT-A-COUNT METHAMPHETAMIN #TKMA1?

The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COAT-A-COUNT METHAMPHETAMIN #TKMA1?

The FDA product code for COAT-A-COUNT METHAMPHETAMIN #TKMA1 is LAF.

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 Diagnostic Products Corp. 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 321 devices →

Related Devices (Code: LAF)

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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