THE SCREENER GSI 55 ABR SCREENER— 510(k) K870030
Substantially EquivalentGrason-Stadler, Inc.
FDA 510(k) clearance K870030 for THE SCREENER GSI 55 ABR SCREENER, Substantially Equivalent on 1987-03-13. Applicant: Grason-Stadler, Inc.. Device class: 2.
Clearance details
- Applicant
- Grason-Stadler, Inc.
- Product code
- Code GWJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1900
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Littleton, MA, US
Recent devices under product code GWJ
view allMore clearances from Grason-Stadler, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.