510(k) K820468

PROFILE GENERAL SET ASSAYED SERUM CONTR by General Diagnostics — Product Code DIF

K820468 is an FDA 510(k) premarket notification submitted by General Diagnostics for the device "PROFILE GENERAL SET ASSAYED SERUM CONTR". The FDA issued a decision of Substantially Equivalent on March 25, 1982. The device falls under product code DIF (Drug Mixture Control Materials), a Class I device regulated under 21 CFR 862.3280. General Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 25, 1982
Date Received
February 22, 1982
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