ECHOPULSE MUSCLE STIMULATOR SYSTEM, MODEL 800— 510(k) K023230
Substantially EquivalentWestern Clinical Technology Systems, Inc.
FDA 510(k) clearance K023230 for ECHOPULSE MUSCLE STIMULATOR SYSTEM, MODEL 800, Substantially Equivalent on 2003-05-05. Applicant: Western Clinical Technology Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Western Clinical Technology Systems, 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
- San Antonio, TX, US
Recent devices under product code IPF
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