510(k) K823303

QUILL CATHETER GUIDE by Medigroup — Product Code FKX

K823303 is an FDA 510(k) premarket notification submitted by Medigroup for the device "QUILL CATHETER GUIDE". The FDA issued a decision of Substantially Equivalent on January 26, 1983. The device falls under product code FKX (System, Peritoneal, Automatic Delivery), a Class II device regulated under 21 CFR 876.5630. Medigroup has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 26, 1983
Date Received
November 5, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Peritoneal, Automatic Delivery
Device Class
Class II
Regulation Number
876.5630
Review Panel
GU
Submission Type