510(k) K914591
K914591 is an FDA 510(k) premarket notification submitted by Stiefel Research Institute, Inc. for the device "L.C.S. 2000 SYSTEM". The FDA issued a decision of Substantially Equivalent on January 14, 1992. The device falls under product code GEH (Unit, Cryosurgical, Accessories), a Class II device regulated under 21 CFR 878.4350. Stiefel Research Institute, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 14, 1992
- Date Received
- October 16, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Cryosurgical, Accessories
- Device Class
- Class II
- Regulation Number
- 878.4350
- Review Panel
- SU
- Submission Type