Last synced on 22 September 2023 at 11:04 pm

Laparoscope (21033FA, 21033FC, 21033WA, 21033WC, 20533FA, 20533FC, 20533WA, 20533WC)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231003
510(k) Type
Traditional
Applicant
Guangdong OptoMedic Technologies, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/6/2023
Days to Decision
90 days
Submission Type
Summary

Laparoscope (21033FA, 21033FC, 21033WA, 21033WC, 20533FA, 20533FC, 20533WA, 20533WC)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231003
510(k) Type
Traditional
Applicant
Guangdong OptoMedic Technologies, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/6/2023
Days to Decision
90 days
Submission Type
Summary