510(k) K955835
K955835 is an FDA 510(k) premarket notification submitted by Instrument Makar, Inc. for the device "FLUID BARRIER BOOT KNEE & ANKLE-HIGH". The FDA issued a decision of Substantially Equivalent on November 19, 1996. The device falls under product code FXP (Cover, Shoe, Operating-Room), a Class I device regulated under 21 CFR 878.4040. Instrument Makar, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 19, 1996
- Date Received
- December 26, 1995
- 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