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FDA 510(k)

NIDA-5/RT, DRUG OF ABUSE CONTROLS

K-Number: K942041 · 1994-09-14

ApplicantMeditech
Decision Date1994-09-14
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

NIDA-5/RT, DRUG OF ABUSE CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Meditech. It received FDA 510(k) clearance on 1994-09-14 under 510(k) number K942041. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIDA-5/RT, DRUG OF ABUSE CONTROLS?

NIDA-5/RT, DRUG OF ABUSE CONTROLS is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is Meditech. The 510(k) number is K942041.

When did NIDA-5/RT, DRUG OF ABUSE CONTROLS receive FDA 510(k) clearance?

NIDA-5/RT, DRUG OF ABUSE CONTROLS received FDA 510(k) clearance on 1994-09-14, under 510(k) number K942041.

Who is the listed applicant for NIDA-5/RT, DRUG OF ABUSE CONTROLS?

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

What is the FDA product code for NIDA-5/RT, DRUG OF ABUSE CONTROLS?

The FDA product code for NIDA-5/RT, DRUG OF ABUSE CONTROLS is DIF.

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Related Devices (Code: DIF)

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.

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Official Source

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