510(k) K884177

DRUG STANDARD SET by Gelman Sciences, Inc. — Product Code DKB

K884177 is an FDA 510(k) premarket notification submitted by Gelman Sciences, Inc. for the device "DRUG STANDARD SET". The FDA issued a decision of Substantially Equivalent on February 17, 1989. The device falls under product code DKB (Calibrators, Drug Mixture), a Class II device regulated under 21 CFR 862.3200. Gelman Sciences, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 17, 1989
Date Received
October 4, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrators, Drug Mixture
Device Class
Class II
Regulation Number
862.3200
Review Panel
TX
Submission Type