NEUROSIGN MODEL 100
FDA 510(k) clearance K923056 · decided 1992-11-24
Clearance details
- K-number
- K923056
- Device name
- NEUROSIGN MODEL 100
- Applicant
- The Magstim Company , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1992-06-24
- Decision date
- 1992-11-24
- Days to decision
- 153 days
- Clearance type
- Traditional
- Product code
- ETN
- Device class
- 2
- Regulation number
- 874.1820
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Carmarthenshire, GB
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.