FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MEDISONIC OXYGEN FLOW CONTROLLER
K Number: K923660
·
Decision Jan 27, 1993
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
70
Applicant Total
5
Review Days
189
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Basic Information
- Device Name
- MEDISONIC OXYGEN FLOW CONTROLLER
- K Number
- K923660
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5905
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Medisonic U.S.A., Inc.
- Date Received
- July 22, 1992
- Decision Date
- January 27, 1993
- Product Code
- NFB
- 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 |
|---|---|---|---|
| NFB | Conserver, Oxygen | FDA class 2 | Anesthesiology |
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