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RUSCH SUPRAFLEX SUPRAPUBIC CYSTOSTOMY CATHETER KIT, STERILE

Page Type
Cleared 510(K)
510(k) Number
K952187
510(k) Type
Traditional
Applicant
RUSCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1995
Days to Decision
77 days
Submission Type
Summary

RUSCH SUPRAFLEX SUPRAPUBIC CYSTOSTOMY CATHETER KIT, STERILE

Page Type
Cleared 510(K)
510(k) Number
K952187
510(k) Type
Traditional
Applicant
RUSCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1995
Days to Decision
77 days
Submission Type
Summary