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DEVICE, FEMALE INCONTINENCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781863
510(k) Type
Traditional
Applicant
ESCHMANN BROS. & WALSH LTD.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
11/6/1978
Days to Decision
0 days

DEVICE, FEMALE INCONTINENCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781863
510(k) Type
Traditional
Applicant
ESCHMANN BROS. & WALSH LTD.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
11/6/1978
Days to Decision
0 days