FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ACTIWATCH
K Number: K983533
·
Decision Mar 23, 1999
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
5
Review Days
166
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Basic Information
- Device Name
- ACTIWATCH
- K Number
- K983533
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Mini-Mitter Co., Inc.
- Date Received
- October 8, 1998
- Decision Date
- March 23, 1999
- Product Code
- GWQ
- 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 |
|---|---|---|---|
| GWQ | Full-Montage Standard Electroencephalograph | FDA class 2 | Neurology |
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