510(k) K802286

ARGLE LATEX PENROSE TUBING by Sherwood Medical Co. — Product Code KGZ

K802286 is an FDA 510(k) premarket notification submitted by Sherwood Medical Co. for the device "ARGLE LATEX PENROSE TUBING". The FDA issued a decision of Substantially Equivalent on October 23, 1980. The device falls under product code KGZ (Accessories, Catheter), a Class I device regulated under 21 CFR 878.4200. Sherwood Medical Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 23, 1980
Date Received
September 19, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessories, Catheter
Device Class
Class I
Regulation Number
878.4200
Review Panel
SU
Submission Type