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KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043114
510(k) Type
Special
Applicant
KIMBERLY-CLARK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
30 days
Submission Type
Statement