510(k) K812368

RAT BLOOD IN ALSEVER'S, CITRATED by Dutchland Laboratories, Inc. — Product Code LHT

K812368 is an FDA 510(k) premarket notification submitted by Dutchland Laboratories, Inc. for the device "RAT BLOOD IN ALSEVER'S, CITRATED". The FDA issued a decision of Substantially Equivalent on September 9, 1981. The device falls under product code LHT (Staphylococcus Aureus Somatic Antigens), a Class I device regulated under 21 CFR 866.3700. Dutchland Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 9, 1981
Date Received
August 20, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Staphylococcus Aureus Somatic Antigens
Device Class
Class I
Regulation Number
866.3700
Review Panel
MI
Submission Type