FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RESPI-PAK RT-PAK
K Number: K910452
·
Decision Apr 16, 1991
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
14
Review Days
74
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Basic Information
- Device Name
- RESPI-PAK RT-PAK
- K Number
- K910452
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.1840
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Cns, Inc.
- Date Received
- February 1, 1991
- Decision Date
- April 16, 1991
- Product Code
- BZG
- 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 |
|---|---|---|---|
| BZG | Spirometer, Diagnostic | FDA class 2 | Anesthesiology |
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