Last synced on 30 May 2025 at 11:05 pm

PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982885
510(k) Type
Traditional
Applicant
SHANGHAI POSEIDON PLASTIC PRODUCTS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1998
Days to Decision
109 days
Submission Type
Statement

PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982885
510(k) Type
Traditional
Applicant
SHANGHAI POSEIDON PLASTIC PRODUCTS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1998
Days to Decision
109 days
Submission Type
Statement