Last synced on 2 December 2022 at 11:04 pm

Single Use Guide Sheath Kit-401, K-402

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212667
510(k) Type
Special
Applicant
Olympus Medical Systems Corp.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
9/22/2021
Days to Decision
30 days
Submission Type
Summary

Single Use Guide Sheath Kit-401, K-402

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212667
510(k) Type
Special
Applicant
Olympus Medical Systems Corp.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
9/22/2021
Days to Decision
30 days
Submission Type
Summary