510(k) K905457

CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL by Consolidated Technologies, Inc. — Product Code DIF

K905457 is an FDA 510(k) premarket notification submitted by Consolidated Technologies, Inc. for the device "CLINICAL CHEMISTRY QUALITY CONTROL MATERIAL". The FDA issued a decision of Substantially Equivalent on April 16, 1991. The device falls under product code DIF (Drug Mixture Control Materials), a Class I device regulated under 21 CFR 862.3280. Consolidated Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 16, 1991
Date Received
December 5, 1990
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