510(k) K961699
K961699 is an FDA 510(k) premarket notification submitted by United States Surgical, A Division of Tyco Healthc for the device "EQUIPMENT COVERS". The FDA issued a decision of Substantially Equivalent on August 23, 1996. The device falls under product code MMP (Cover, Barrier, Protective), a Class II device regulated under 21 CFR 878.4370. United States Surgical, A Division of Tyco Healthc has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 23, 1996
- Date Received
- May 2, 1996
- 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