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PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892086
510(k) Type
Traditional
Applicant
CYPRESS MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1989
Days to Decision
31 days

PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892086
510(k) Type
Traditional
Applicant
CYPRESS MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1989
Days to Decision
31 days