FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
OHMEDA MODEL 0001/0003 RECORDER
K Number: K851274
·
Decision May 15, 1985
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
86
Applicant Total
120
Review Days
44
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Basic Information
- Device Name
- OHMEDA MODEL 0001/0003 RECORDER
- K Number
- K851274
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 870.2810
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Ohmeda Medical
- Date Received
- April 1, 1985
- Decision Date
- May 15, 1985
- Product Code
- DSF
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DSF | Recorder, Paper Chart | FDA class 1 | Cardiovascular |
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|---|---|---|---|
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| 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 |