510(k) K791106

STERILE, DISPOSABLE CENTRIFUGE BOWL by Travenol Laboratories, S.A. — Product Code GKT

K791106 is an FDA 510(k) premarket notification submitted by Travenol Laboratories, S.A. for the device "STERILE, DISPOSABLE CENTRIFUGE BOWL". The FDA issued a decision of Substantially Equivalent on August 10, 1979. The device falls under product code GKT (Separator, Automated, Blood Cell, Diagnostic), a Class II device regulated under 21 CFR 864.9245. Travenol Laboratories, S.A. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 10, 1979
Date Received
June 13, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Separator, Automated, Blood Cell, Diagnostic
Device Class
Class II
Regulation Number
864.9245
Review Panel
HE
Submission Type