510(k) K010222
K010222 is an FDA 510(k) premarket notification submitted by Ohmeda Medical for the device "OHMEDA MEDICAL GIRAFFE INCUBATOR". The FDA issued a decision of Substantially Equivalent on March 21, 2001. The device falls under product code FMZ (Incubator, Neonatal), a Class II device regulated under 21 CFR 880.5400. Ohmeda Medical has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 21, 2001
- Date Received
- January 24, 2001
- 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