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CUTIPLAST STERIL

Page Type
Cleared 510(K)
510(k) Number
K943363
510(k) Type
Traditional
Applicant
BEIERSDORF, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1995
Days to Decision
245 days
Submission Type
Summary

CUTIPLAST STERIL

Page Type
Cleared 510(K)
510(k) Number
K943363
510(k) Type
Traditional
Applicant
BEIERSDORF, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1995
Days to Decision
245 days
Submission Type
Summary