510(k) K914702

STERILE VIEW(TM) KNEE-HIGH BOOTS/DEPUY SHOE BOOTS by Depuy, Inc. — Product Code FXP

K914702 is an FDA 510(k) premarket notification submitted by Depuy, Inc. for the device "STERILE VIEW(TM) KNEE-HIGH BOOTS/DEPUY SHOE BOOTS". The FDA issued a decision of Substantially Equivalent on January 29, 1993. The device falls under product code FXP (Cover, Shoe, Operating-Room), a Class I device regulated under 21 CFR 878.4040. Depuy, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 29, 1993
Date Received
October 18, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cover, Shoe, Operating-Room
Device Class
Class I
Regulation Number
878.4040
Review Panel
HO
Submission Type