FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE
K Number: K963704
·
Decision Nov 26, 1996
Classifications
1
FEI Numbers
176
Registration Numbers
176
Same Product Code
12
Applicant Total
13
Review Days
71
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Basic Information
- Device Name
- MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE
- K Number
- K963704
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.5660
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Shippert Medical Technologies Corp.
- Date Received
- September 16, 1996
- Decision Date
- November 26, 1996
- Product Code
- LYG
- 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 |
|---|---|---|---|
| LYG | Massager, Therapeutic, Manual | FDA class 1 | Physical Medicine |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LYG), ordered by most recent decision date.
MANUAL MASSAGE ROLLER
FDA 510(k)
FDA Class 1
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BACK MASSAGER
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FDA Class 1
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HOOKING SYSTEM
FDA 510(k)
FDA Class 1
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STRESS HANDLER
FDA 510(k)
FDA Class 1
·Physical Medicine
THE MASSAGER
FDA 510(k)
FDA Class 1
·Physical Medicine
SPINE LINE
FDA 510(k)
FDA Class 1
·Physical Medicine
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