510(k) K820454

THE RED CAP by Burron Medical Products, Inc. — Product Code FMF

K820454 is an FDA 510(k) premarket notification submitted by Burron Medical Products, Inc. for the device "THE RED CAP". The FDA issued a decision of Substantially Equivalent on March 8, 1982. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Burron Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 8, 1982
Date Received
February 18, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Piston
Device Class
Class II
Regulation Number
880.5860
Review Panel
HO
Submission Type