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UST-5522-7.5 & UST-5522L-7.5 INTRAOPERATIVE TRANS.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925486
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
105 days
Submission Type
Statement

UST-5522-7.5 & UST-5522L-7.5 INTRAOPERATIVE TRANS.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925486
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
105 days
Submission Type
Statement