PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE— 510(k) K982885
Substantially EquivalentShanghai Poseidon Plastic Products Co., Ltd.
FDA 510(k) clearance K982885 for PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE, Substantially Equivalent on 1998-12-04. Applicant: Shanghai Poseidon Plastic Products Co., Ltd..
Clearance details
- Applicant
- Shanghai Poseidon Plastic Products Co., Ltd.
- Product code
- Code LYZ
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palm Harbor, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.