AESCULAP VENTRICULOSCOPE SYSTEM
FDA 510(k) clearance K954394 · decided 1996-03-07
Clearance details
- K-number
- K954394
- Device name
- AESCULAP VENTRICULOSCOPE SYSTEM
- Applicant
- Aesculap, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1995-09-18
- Decision date
- 1996-03-07
- Days to decision
- 171 days
- Clearance type
- Traditional
- Product code
- GWG
- Device class
- 2
- Regulation number
- 882.1480
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- South San Francisco, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.