Last synced on 9 May 2025 at 11:05 pm

PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891662
510(k) Type
Traditional
Applicant
DARCHET (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1990
Days to Decision
312 days

PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891662
510(k) Type
Traditional
Applicant
DARCHET (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1990
Days to Decision
312 days