FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MINITROP AEROSAL, PRODOMO AEROSAL AND
K Number: K830913
·
Decision May 25, 1983
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
220
Applicant Total
5
Review Days
65
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Basic Information
- Device Name
- MINITROP AEROSAL, PRODOMO AEROSAL AND
- K Number
- K830913
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5450
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Medlog GmbH Marketing Services
- Date Received
- March 21, 1983
- Decision Date
- May 25, 1983
- Product Code
- BTT
- 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 |
|---|---|---|---|
| BTT | Humidifier, Respiratory Gas, (Direct Patient Interface) | FDA class 2 | Anesthesiology |
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