Last synced on 30 May 2025 at 11:05 pm

VINYL EXAMINATION GLOVE, POWDER-FREE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944510
510(k) Type
Traditional
Applicant
AMERICAN GEMINI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1994
Days to Decision
33 days
Submission Type
Statement

VINYL EXAMINATION GLOVE, POWDER-FREE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944510
510(k) Type
Traditional
Applicant
AMERICAN GEMINI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1994
Days to Decision
33 days
Submission Type
Statement