510(k) K823648

SURGICAL TUBING by Fred Sammons, Inc. — Product Code IOD

K823648 is an FDA 510(k) premarket notification submitted by Fred Sammons, Inc. for the device "SURGICAL TUBING". The FDA issued a decision of Substantially Equivalent on January 21, 1983. The device falls under product code IOD (Components, Exercise), a Class I device regulated under 21 CFR 890.5350. Fred Sammons, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 21, 1983
Date Received
December 6, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Components, Exercise
Device Class
Class I
Regulation Number
890.5350
Review Panel
PM
Submission Type