510(k) K914702
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