ECHOENCEPHALOGRAPH, DIGITAL, 1000— 510(k) K770575
Substantially EquivalentStorz Instrument Co.
FDA 510(k) clearance K770575 for ECHOENCEPHALOGRAPH, DIGITAL, 1000, Substantially Equivalent on 1977-04-26. Applicant: Storz Instrument Co..
Clearance details
- Applicant
- Storz Instrument Co.
- Product code
- Code GXW
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.