Last synced on 25 January 2026 at 3:41 am

PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892774
510(k) Type
Traditional
Applicant
LIAONING-USA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1989
Days to Decision
155 days

PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892774
510(k) Type
Traditional
Applicant
LIAONING-USA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1989
Days to Decision
155 days