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BLADDER CATH KIT W/OUT CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780268
510(k) Type
Traditional
Applicant
LATEX IND., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1978
Days to Decision
7 days

BLADDER CATH KIT W/OUT CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780268
510(k) Type
Traditional
Applicant
LATEX IND., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1978
Days to Decision
7 days