510(k) K942257

DOA-PLUS, DRUGS OF ABUSE CONTROLS by Medical Diagnostic Technologies, Inc. — Product Code DIF

K942257 is an FDA 510(k) premarket notification submitted by Medical Diagnostic Technologies, Inc. for the device "DOA-PLUS, DRUGS OF ABUSE CONTROLS". The FDA issued a decision of Substantially Equivalent on September 14, 1994. The device falls under product code DIF (Drug Mixture Control Materials), a Class I device regulated under 21 CFR 862.3280. Medical Diagnostic Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1994
Date Received
May 9, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drug Mixture Control Materials
Device Class
Class I
Regulation Number
862.3280
Review Panel
TX
Submission Type