BIOREHAB SYSTEM— 510(k) K011823
Substantially EquivalentNicolet Biomedical, Inc.
FDA 510(k) clearance K011823 for BIOREHAB SYSTEM, Substantially Equivalent on 2001-09-06. Applicant: Nicolet Biomedical, Inc.. Device class: 2.
Clearance details
- Applicant
- Nicolet Biomedical, Inc.
- Product code
- Code HCC
- Device class
- Class 2
- Regulation
- 21 CFR 882.5050
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Stoughton, WI, US
Recent devices under product code HCC
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