510(k) K941752

SPECTROLYSE ANTIPLASMIN KIT by Biopool AB — Product Code GGP

K941752 is an FDA 510(k) premarket notification submitted by Biopool AB for the device "SPECTROLYSE ANTIPLASMIN KIT". The FDA issued a decision of Substantially Equivalent (kit) on September 25, 1995. The device falls under product code GGP (Test, Qualitative And Quantitative Factor Deficiency), a Class II device regulated under 21 CFR 864.7290. Biopool AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESK (Substantially Equivalent (kit))
Decision Date
September 25, 1995
Date Received
April 8, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Test, Qualitative And Quantitative Factor Deficiency
Device Class
Class II
Regulation Number
864.7290
Review Panel
HE
Submission Type