Last synced on 25 January 2026 at 3:41 am

MERIDIAN-II AND MERDIAN-PLUS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001347
510(k) Type
Traditional
Applicant
Meridian Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/3/2000
Days to Decision
189 days
Submission Type
Summary

MERIDIAN-II AND MERDIAN-PLUS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001347
510(k) Type
Traditional
Applicant
Meridian Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/3/2000
Days to Decision
189 days
Submission Type
Summary