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4K UHD Laparoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203255
510(k) Type
Traditional
Applicant
Scivita Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/24/2021
Days to Decision
112 days
Submission Type
Summary