FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
VIBRA-SURGE SYSTEM MODEL VS2120
K Number: K971533
·
Decision Jul 25, 1997
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
156
Applicant Total
1
Review Days
88
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Basic Information
- Device Name
- VIBRA-SURGE SYSTEM MODEL VS2120
- K Number
- K971533
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Sonics & Materials, Inc.
- Date Received
- April 28, 1997
- Decision Date
- July 25, 1997
- Product Code
- LFL
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| LFL | Instrument, Ultrasonic Surgical | FDA unclassified | Unknown |
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