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SINGLE USE 3-LUMEN BALLOON CATHETER, MODELS B-230Q-A AND B-230Q-B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033333
510(k) Type
Special
Applicant
AOMORI OLYMPUS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2003
Days to Decision
29 days
Submission Type
Summary

SINGLE USE 3-LUMEN BALLOON CATHETER, MODELS B-230Q-A AND B-230Q-B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033333
510(k) Type
Special
Applicant
AOMORI OLYMPUS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2003
Days to Decision
29 days
Submission Type
Summary