ELECTROFLEX— 510(k) K943126
Substantially EquivalentMedical Devices, Inc.
FDA 510(k) clearance K943126 for ELECTROFLEX, Substantially Equivalent on 1994-12-05. Applicant: Medical Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Medical Devices, Inc.
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
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More clearances from Medical Devices, Inc.
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