MYOPAC (TM), MODEL 9600— 510(k) K864625
Substantially Equivalent for Some IndicationsMedical Devices, Inc.
FDA 510(k) clearance K864625 for MYOPAC (TM), MODEL 9600, Substantially Equivalent for Some Indications on 1986-12-29. Applicant: Medical Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Medical Devices, Inc.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
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