Last synced on 16 May 2025 at 11:05 pm

AMBIDERM(TM) PATIENT EXAMINATION GLOVE (LATEX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891298
510(k) Type
Traditional
Applicant
MEDI TEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1989
Days to Decision
16 days

AMBIDERM(TM) PATIENT EXAMINATION GLOVE (LATEX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891298
510(k) Type
Traditional
Applicant
MEDI TEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1989
Days to Decision
16 days