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UROGRAM CYSTOMETROGRAM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936041
510(k) Type
Traditional
Applicant
MYO/KINETIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1994
Days to Decision
119 days
Submission Type
Statement

UROGRAM CYSTOMETROGRAM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936041
510(k) Type
Traditional
Applicant
MYO/KINETIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1994
Days to Decision
119 days
Submission Type
Statement