510(k) K951800

CMV IGG HUMAN SERUM CONTROLS by Pyramid Biological Corp. — Product Code GQI

K951800 is an FDA 510(k) premarket notification submitted by Pyramid Biological Corp. for the device "CMV IGG HUMAN SERUM CONTROLS". The FDA issued a decision of Substantially Equivalent on November 16, 1995. The device falls under product code GQI (Antiserum, Cf, Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. Pyramid Biological Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 16, 1995
Date Received
April 18, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antiserum, Cf, Cytomegalovirus
Device Class
Class II
Regulation Number
866.3175
Review Panel
MI
Submission Type