MERIDIAN-PORTABLE— 510(k) K010897
Substantially EquivalentMeridian Co., Ltd.
FDA 510(k) clearance K010897 for MERIDIAN-PORTABLE, Substantially Equivalent on 2001-06-19. Applicant: Meridian Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Meridian Co., Ltd.
- Product code
- Code GZO
- Device class
- Class 2
- Regulation
- 21 CFR 882.1540
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Songpa-Gu, Seoul, KR
Recent devices under product code GZO
view allMore clearances from Meridian Co., Ltd.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.