PROGEL (TM) DUAL ELECTRODE PAD, MODEL 8535— 510(k) K882886
Substantially EquivalentMedical Devices, Inc.
FDA 510(k) clearance K882886 for PROGEL (TM) DUAL ELECTRODE PAD, MODEL 8535, Substantially Equivalent on 1988-09-29. 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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