FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PFLEX TM
K Number: K820528
·
Decision Mar 26, 1982
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
4
Review Days
25
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Basic Information
- Device Name
- PFLEX TM
- K Number
- K820528
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5690
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Health Scan, Inc.
- Date Received
- March 1, 1982
- Decision Date
- March 26, 1982
- Product Code
- BWF
- 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 |
|---|---|---|---|
| BWF | Spirometer, Therapeutic (Incentive) | FDA class 2 | Anesthesiology |
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