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ENDOSCOPICALLY DELIVERALBE ULTRASOUND POINT PORBE SYSTEM (ENDOSCOPY)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971528
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/1997
Days to Decision
228 days
Submission Type
Statement

ENDOSCOPICALLY DELIVERALBE ULTRASOUND POINT PORBE SYSTEM (ENDOSCOPY)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971528
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/1997
Days to Decision
228 days
Submission Type
Statement