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MODIFIED MULTI-LUMEN NASOGASTRIC TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871691
510(k) Type
Traditional
Applicant
BISSELL MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1987
Days to Decision
103 days

MODIFIED MULTI-LUMEN NASOGASTRIC TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871691
510(k) Type
Traditional
Applicant
BISSELL MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1987
Days to Decision
103 days