Shanghai Poseidon Plastic Products Co., Ltd. · Class I · Cleared Dec 4, 1998
| K-number | K982885 |
| Device name | PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE |
| Applicant | Shanghai Poseidon Plastic Products Co., Ltd. |
| Product code | LYZ |
| Device class | Class I |
| Decision date | Dec 4, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 880.6250 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov