FEEDBACK EMG SYSTEM, MODEL PE-L00— 510(k) K770663
Substantially EquivalentBio-Feedback Systems, Inc.
FDA 510(k) clearance K770663 for FEEDBACK EMG SYSTEM, MODEL PE-L00, Substantially Equivalent on 1977-04-26. Applicant: Bio-Feedback Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Bio-Feedback Systems, 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
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code HCC
view allMore clearances from Bio-Feedback Systems, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.