FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
OHMEDA 5500 AIRWAY PRESSURE MONITOR
K Number: K864536
·
Decision Jan 12, 1987
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
120
Review Days
56
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Basic Information
- Device Name
- OHMEDA 5500 AIRWAY PRESSURE MONITOR
- K Number
- K864536
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.2600
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Ohmeda Medical
- Date Received
- November 17, 1986
- Decision Date
- January 12, 1987
- Product Code
- CAP
- 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 |
|---|---|---|---|
| CAP | Monitor, Airway Pressure (Includes Gauge And/Or Alarm) | FDA class 2 | Anesthesiology |
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| K040068 | BILIBLANKET PLUS HIGH OUTPUT PHOTOTHERAPY SYSTEM | Apr 16, 2004 | Substantially Equivalent |
| K020543 | OHMEDA MEDICAL GIRAFFE OMNIBED | May 9, 2002 | Substantially Equivalent |