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LM-9300 Plus Lithotripter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213772
510(k) Type
Traditional
Applicant
Lite-Med Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
1/19/2023
Days to Decision
413 days
Submission Type
Summary

LM-9300 Plus Lithotripter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213772
510(k) Type
Traditional
Applicant
Lite-Med Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
1/19/2023
Days to Decision
413 days
Submission Type
Summary