FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DISCIPLINE I
K Number: K870872
·
Decision Mar 23, 1987
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
60
Applicant Total
3
Review Days
20
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Basic Information
- Device Name
- DISCIPLINE I
- K Number
- K870872
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5360
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Physio Systems, Inc.
- Date Received
- March 3, 1987
- Decision Date
- March 23, 1987
- Product Code
- ISD
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| ISD | Exerciser, Measuring | FDA class 2 | Physical Medicine |
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