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MODIFICATION OF PURESPERM

Page Type
Cleared 510(K)
510(k) Number
K984172
510(k) Type
Traditional
Applicant
NIDACON INTERNATIONAL AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/1999
Days to Decision
55 days
Submission Type
Summary

MODIFICATION OF PURESPERM

Page Type
Cleared 510(K)
510(k) Number
K984172
510(k) Type
Traditional
Applicant
NIDACON INTERNATIONAL AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/1999
Days to Decision
55 days
Submission Type
Summary