Last synced on 16 May 2025 at 11:05 pm

LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913033
510(k) Type
Traditional
Applicant
REAGENT HOSPITAL PROD. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1991
Days to Decision
29 days
Submission Type
Statement

LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913033
510(k) Type
Traditional
Applicant
REAGENT HOSPITAL PROD. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1991
Days to Decision
29 days
Submission Type
Statement