510(k) K912838

BARTELS RESPIRATORY SYNCYTIAL VIRUS ENZYME IMMUNO by Baxter Diagnostics, Inc. — Product Code LKT

K912838 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "BARTELS RESPIRATORY SYNCYTIAL VIRUS ENZYME IMMUNO". The FDA issued a decision of Substantially Equivalent on September 27, 1991. The device falls under product code LKT (Respiratory Syncytial Virus, Antigen, Antibody, Ifa), a Class I device regulated under 21 CFR 866.3480. Baxter Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 27, 1991
Date Received
June 26, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Respiratory Syncytial Virus, Antigen, Antibody, Ifa
Device Class
Class I
Regulation Number
866.3480
Review Panel
MI
Submission Type