SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST
K-Number: K000273 · 2000-04-07
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Device Summary
Frequently Asked Questions
What is the SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST?
SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST is a medical device that received FDA 510(k) clearance on 2000-04-07. The listed applicant is Drug Detection Devices, Ltd.. The 510(k) number is K000273.
When did SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST receive FDA 510(k) clearance?
SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST received FDA 510(k) clearance on 2000-04-07, under 510(k) number K000273.
Who is the listed applicant for SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST?
The FDA 510(k) record lists Drug Detection Devices, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST?
The FDA product code for SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST is DJG.
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 Drug Detection Devices, Ltd. 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.
Related Devices (Code: DJG)
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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