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GERSON 2130/31 TYPE N95 NIOSH CERTIFIED SURGICAL RESPIRATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050193
510(k) Type
Traditional
Applicant
LOUIS M. GERSON CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2005
Days to Decision
74 days
Submission Type
Statement

GERSON 2130/31 TYPE N95 NIOSH CERTIFIED SURGICAL RESPIRATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050193
510(k) Type
Traditional
Applicant
LOUIS M. GERSON CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2005
Days to Decision
74 days
Submission Type
Statement