510(k) K761118

HAND SCREW CLAMP by Fred Sammons, Inc. — Product Code IOD

K761118 is an FDA 510(k) premarket notification submitted by Fred Sammons, Inc. for the device "HAND SCREW CLAMP". The FDA issued a decision of Substantially Equivalent on December 2, 1976. 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
December 2, 1976
Date Received
November 19, 1976
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