510(k) K841665

RHESUS SV5/SV40 by Viromed Laboratories, Inc. — Product Code KIR

K841665 is an FDA 510(k) premarket notification submitted by Viromed Laboratories, Inc. for the device "RHESUS SV5/SV40". The FDA issued a decision of Substantially Equivalent on May 7, 1984. The device falls under product code KIR (Cells, Animal And Human, Cultured), a Class I device regulated under 21 CFR 864.2280. Viromed Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 7, 1984
Date Received
April 23, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cells, Animal And Human, Cultured
Device Class
Class I
Regulation Number
864.2280
Review Panel
PA
Submission Type