FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ELECTRIC MUSCLE STIMULATOR
K Number: K813533
·
Decision Mar 5, 1982
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
8
Review Days
78
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Basic Information
- Device Name
- ELECTRIC MUSCLE STIMULATOR
- K Number
- K813533
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5850
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Myo-Tronics Research, Inc.
- Date Received
- December 17, 1981
- Decision Date
- March 5, 1982
- Product Code
- IPF
- 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 |
|---|---|---|---|
| IPF | Stimulator, Muscle, Powered | FDA class 2 | Physical Medicine |
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Other Clearances by Myo-Tronics Research, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K842223 | J4 MYO-MONITOR | Nov 19, 1984 | Substantially Equivalent |
| K842224 | BNS 40 | Nov 19, 1984 | Substantially Equivalent |
| K833132 | MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY | Feb 10, 1984 | Substantially Equivalent |
| K831364 | TESTCORP RA | May 27, 1983 | Substantially Equivalent |
| K830034 | MODEL EM-2 BIOELECTRIC PROCESSOR | Feb 9, 1983 | Substantially Equivalent |
| K810528 | MODEL EM-IR | Mar 31, 1981 | Substantially Equivalent |
| K770252 | MONITOR, MYO, MODEL J3 | Feb 18, 1977 | Substantially Equivalent |