The following data is part of a premarket notification filed by Shanghai Poseidon Plastic Products Co., Ltd. with the FDA for Shanghai Posedon Plastic Products Vinyl Exam Gloves.
Device ID | K954381 |
510k Number | K954381 |
Device Name: | SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES |
Classification | Vinyl Patient Examination Glove |
Applicant | SHANGHAI POSEIDON PLASTIC PRODUCTS CO., LTD. 202 SOUTH ROUTE 31 Mchenry, IL 60050 |
Contact | Anthony L Giaccio |
Correspondent | Anthony L Giaccio SHANGHAI POSEIDON PLASTIC PRODUCTS CO., LTD. 202 SOUTH ROUTE 31 Mchenry, IL 60050 |
Product Code | LYZ |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-09-19 |
Decision Date | 1995-12-11 |