510(k) K820581

NORTON JUGULAR KITS by Norton Performance Plastics Corp. — Product Code DYB

K820581 is an FDA 510(k) premarket notification submitted by Norton Performance Plastics Corp. for the device "NORTON JUGULAR KITS". The FDA issued a decision of Substantially Equivalent on March 18, 1982. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Norton Performance Plastics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 18, 1982
Date Received
March 4, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Introducer, Catheter
Device Class
Class II
Regulation Number
870.1340
Review Panel
CV
Submission Type