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LEEDAR (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
K891663
510(k) Type
Traditional
Applicant
DARCHET (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1990
Days to Decision
330 days

LEEDAR (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
K891663
510(k) Type
Traditional
Applicant
DARCHET (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1990
Days to Decision
330 days