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.. Device class: 2.
Clearance details
- Applicant
- Storz Instrument Co.
- Product code
- Code GXW
- Device class
- Class 2
- Regulation
- 21 CFR 882.1240
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.