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SPOROX

Page Type
Cleared 510(K)
510(k) Number
K970230
510(k) Type
Traditional
Applicant
RECKITT BENCKISER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1997
Days to Decision
281 days
Submission Type
Summary

SPOROX

Page Type
Cleared 510(K)
510(k) Number
K970230
510(k) Type
Traditional
Applicant
RECKITT BENCKISER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1997
Days to Decision
281 days
Submission Type
Summary