FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CDX 200
K Number: K820035
·
Decision Mar 10, 1982
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
25
Applicant Total
4
Review Days
62
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Basic Information
- Device Name
- CDX 200
- K Number
- K820035
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.1900
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Cdx Corp.
- Date Received
- January 7, 1982
- Decision Date
- March 10, 1982
- Product Code
- BZM
- 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 |
|---|---|---|---|
| BZM | Calculator, Pulmonary Function Interpretor (Diagnostic) | FDA class 2 | Anesthesiology |
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