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KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880850
510(k) Type
Traditional
Applicant
KMB MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1988
Days to Decision
86 days

KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880850
510(k) Type
Traditional
Applicant
KMB MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1988
Days to Decision
86 days