510(k) K790084

SURGICAL RULER AND PEN by Devon Industries, Inc. — Product Code FZZ

K790084 is an FDA 510(k) premarket notification submitted by Devon Industries, Inc. for the device "SURGICAL RULER AND PEN". The FDA issued a decision of Substantially Equivalent on February 26, 1979. The device falls under product code FZZ (Marker, Skin), a Class I device regulated under 21 CFR 878.4660. Devon Industries, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 26, 1979
Date Received
January 16, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Marker, Skin
Device Class
Class I
Regulation Number
878.4660
Review Panel
SU
Submission Type