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CROSSTEX ISOLITE AND ISOFLUID EARLOOP FACE MASKS AND ISOFLUID FOGFREE FACE MASKS WITH AND WITHOUT SPLASH VISOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082258
510(k) Type
Traditional
Applicant
CROSSTEX INTERNATIONAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2008
Days to Decision
69 days
Submission Type
Summary

CROSSTEX ISOLITE AND ISOFLUID EARLOOP FACE MASKS AND ISOFLUID FOGFREE FACE MASKS WITH AND WITHOUT SPLASH VISOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082258
510(k) Type
Traditional
Applicant
CROSSTEX INTERNATIONAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2008
Days to Decision
69 days
Submission Type
Summary