Last synced on 4 February 2023 at 10:33 pm

SPERMASSIST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022443
510(k) Type
Traditional
Applicant
NIDACON INTERNATIONAL AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2002
Days to Decision
34 days
Submission Type
Summary

SPERMASSIST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022443
510(k) Type
Traditional
Applicant
NIDACON INTERNATIONAL AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2002
Days to Decision
34 days
Submission Type
Summary