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CONSEAL COLOSTOMY CONTINENCE SYSTEM (ONE-PIECE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881636
510(k) Type
Traditional
Applicant
COLOPLAST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1988
Days to Decision
90 days

CONSEAL COLOSTOMY CONTINENCE SYSTEM (ONE-PIECE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881636
510(k) Type
Traditional
Applicant
COLOPLAST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1988
Days to Decision
90 days