FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
OHMEDA INOVENT DELIVERY SYSTEM
K Number: DEN000001
·
Decision Jan 11, 2000
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
32
Applicant Total
120
Review Days
4
Basic Information
- Device Name
- OHMEDA INOVENT DELIVERY SYSTEM
- K Number
- DEN000001
- Device Class
- FDA class 2
- Clearance Type
- Post-NSE
- Regulation Number
- 868.5165
- Medical Specialty
- Anesthesiology
- Decision
- Unknown
- Applicant
- OHMEDA MEDICAL
- Date Received
- January 7, 2000
- Decision Date
- January 11, 2000
- Product Code
- MRN
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MRN | Apparatus, Nitric Oxide Delivery | FDA class 2 | Anesthesiology |
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Other Clearances by OHMEDA MEDICAL
| K Number | Device Name | ||
|---|---|---|---|
| K123309 | GIRAFFE AND PANDA WARMERS | Feb 5, 2013 | Substantially Equivalent |
| K101788 | GIRAFFE OMNIBED | Jul 21, 2010 | Substantially Equivalent |
| K101778 | GIRAFFE INCUBATOR | Jul 21, 2010 | Substantially Equivalent |
| K090697 | MODIFICATION TO: GIRAFFE AND PANDA WARMER | Apr 16, 2009 | Substantially Equivalent |
| K072157 | MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY) | Aug 27, 2007 | Substantially Equivalent |
| K070377 | GIRAFFE AND PANDA WARMER | Jul 11, 2007 | Substantially Equivalent |
| K070210 | GIRAFFE AND PANDA T- PIECE RESUSCITATION SYSTEM | Apr 20, 2007 | Substantially Equivalent |
| K070247 | GIRAFFE AND PANDA BAG AND MASK RESUSCITATION SYSTEM | Apr 20, 2007 | Substantially Equivalent |
| K040068 | BILIBLANKET PLUS HIGH OUTPUT PHOTOTHERAPY SYSTEM | Apr 16, 2004 | Substantially Equivalent |
| K020543 | OHMEDA MEDICAL GIRAFFE OMNIBED | May 9, 2002 | Substantially Equivalent |