FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DANTEC COUNTERPOINT MK2(TM)
K Number: K913957
·
Decision Jan 30, 1992
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
75
Applicant Total
25
Review Days
148
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Basic Information
- Device Name
- DANTEC COUNTERPOINT MK2(TM)
- K Number
- K913957
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1900
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Dantec Medical, Inc.
- Date Received
- September 4, 1991
- Decision Date
- January 30, 1992
- Product Code
- GWJ
- Advisory Committee
- Neurology
- 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 |
|---|---|---|---|
| GWJ | Stimulator, Auditory, Evoked Response | FDA class 2 | Neurology |
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|---|---|---|---|
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| K953999 | DANTEC DA CAPO | Nov 21, 1995 | Substantially Equivalent |
| K926363 | MULTI-DOP S | Jun 19, 1995 | Substantially Equivalent |
| K931801 | MULTI-DOP X | Jun 14, 1995 | Substantially Equivalent |
| K930458 | MULTI-DOP L | Feb 3, 1995 | Substantially Equivalent |
| K932059 | NEEDLE ELECTRODES AND DISPOSABLE SCALP ELECTRODE | Oct 4, 1994 | Substantially Equivalent |
| K934580 | DANTEC 13R45 BAR ELECTRODE | Sep 26, 1994 | Substantially Equivalent |
| K931966 | DANTEC DISPOSABLE CONCENTRIC NEEDLE | Mar 30, 1994 | Substantially Equivalent |
| K931923 | DANTEC MAGLITE MAGNETIC STIMULATOR (MAGLITE) | Nov 9, 1993 | Substantially Equivalent |