FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RESPI-NEB-AEROSOL SYSTEM
K Number: K830417
·
Decision Mar 24, 1983
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
73
Applicant Total
1
Review Days
44
Basic Information
- Device Name
- RESPI-NEB-AEROSOL SYSTEM
- K Number
- K830417
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.6250
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- PROFESSIONAL MEDICAL SUPPLY, INC.
- Date Received
- February 8, 1983
- Decision Date
- March 24, 1983
- Product Code
- BTI
- 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 |
|---|---|---|---|
| BTI | Compressor, Air, Portable | FDA class 2 | Anesthesiology |
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