FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MYOLAB II, MODEL ML-200
K Number: K862236
·
Decision Aug 7, 1986
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
74
Applicant Total
4
Review Days
57
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Basic Information
- Device Name
- MYOLAB II, MODEL ML-200
- K Number
- K862236
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.1375
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Motion Control, Inc.
- Date Received
- June 11, 1986
- Decision Date
- August 7, 1986
- Product Code
- IKN
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| IKN | Electromyograph, Diagnostic | FDA class 2 | Physical Medicine |
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