510(k) K802339

EIA RUBELLA-G by Beckman Instruments, Inc. — Product Code GOL

K802339 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "EIA RUBELLA-G". The FDA issued a decision of Substantially Equivalent on December 18, 1980. The device falls under product code GOL (Antigen, Ha (Including Ha Control), Rubella), a Class II device regulated under 21 CFR 866.3510. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 18, 1980
Date Received
September 26, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigen, Ha (Including Ha Control), Rubella
Device Class
Class II
Regulation Number
866.3510
Review Panel
MI
Submission Type