510(k) K993051
K993051 is an FDA 510(k) premarket notification submitted by Hill-Rom Air-Shields for the device "VERSALET 7700 CARE CENTER, MODEL # 7700". The FDA issued a decision of Substantially Equivalent on February 3, 2000. The device falls under product code FMZ (Incubator, Neonatal), a Class II device regulated under 21 CFR 880.5400. Hill-Rom Air-Shields has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 3, 2000
- Date Received
- September 13, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Incubator, Neonatal
- Device Class
- Class II
- Regulation Number
- 880.5400
- Review Panel
- HO
- Submission Type