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Pentax Medical Valve Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222980
510(k) Type
Traditional
Applicant
Yangzhou Fartley Medical Instrument Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/21/2022
Days to Decision
54 days
Submission Type
Summary

Pentax Medical Valve Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222980
510(k) Type
Traditional
Applicant
Yangzhou Fartley Medical Instrument Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/21/2022
Days to Decision
54 days
Submission Type
Summary