510(k) K930552
K930552 is an FDA 510(k) premarket notification submitted by Patient Safety Products, Inc. for the device "STERILE BARRIER SLEEVE AND COVER". The FDA issued a decision of Substantially Equivalent on July 5, 1994. The device falls under product code MMP (Cover, Barrier, Protective), a Class II device regulated under 21 CFR 878.4370.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 5, 1994
- Date Received
- February 3, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cover, Barrier, Protective
- Device Class
- Class II
- Regulation Number
- 878.4370
- Review Panel
- HO
- Submission Type