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ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083153
510(k) Type
Traditional
Applicant
Hollister, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/4/2009
Days to Decision
103 days
Submission Type
Summary

ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083153
510(k) Type
Traditional
Applicant
Hollister, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/4/2009
Days to Decision
103 days
Submission Type
Summary