ESCOTEK EST 220 INTERFERENCE THERAPY UNIT— 510(k) K844388
Substantially EquivalentNor-Am Patient Care Products, Inc.
FDA 510(k) clearance K844388 for ESCOTEK EST 220 INTERFERENCE THERAPY UNIT, Substantially Equivalent on 1985-05-07. Applicant: Nor-Am Patient Care Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Nor-Am Patient Care Products, 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
- Clearance type
- Traditional
- Location
- Walker, MI, US
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