MM-1 MOVEMENT MONITOR— 510(k) K971318
Substantially EquivalentAxon Instruments, Inc.
FDA 510(k) clearance K971318 for MM-1 MOVEMENT MONITOR, Substantially Equivalent on 1997-07-28. Applicant: Axon Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Axon Instruments, Inc.
- Product code
- Code GYD
- Device class
- Class 2
- Regulation
- 21 CFR 882.1950
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Foster City, CA, US
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