510(k) K834135

STERILE SUTURE BOOTS by Devon Industries, Inc. — Product Code KDD

K834135 is an FDA 510(k) premarket notification submitted by Devon Industries, Inc. for the device "STERILE SUTURE BOOTS". The FDA issued a decision of Substantially Equivalent on April 27, 1984. The device falls under product code KDD (Kit, Surgical Instrument, Disposable), a Class I device regulated under 21 CFR 878.4800. Devon Industries, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 27, 1984
Date Received
December 1, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Surgical Instrument, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type