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XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860285
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/1986
Days to Decision
14 days

XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860285
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/1986
Days to Decision
14 days