The following data is part of a premarket notification filed by Foshan Nanhai Plus Medical Co., Ltd. with the FDA for Plus Surgical Drapes (eo Sterilized), Pmdb-xxx.
Device ID | K133080 |
510k Number | K133080 |
Device Name: | Plus Surgical Drapes (EO Sterilized), PMDB-XXX |
Classification | Drape, Surgical |
Applicant | FOSHAN NANHAI PLUS MEDICAL CO., LTD. 3500 SOUTH DUPONT HIGHWAY Dover, DE 19901 |
Contact | Leon Lu |
Correspondent | Leon Lu FOSHAN NANHAI PLUS MEDICAL CO., LTD. 3500 SOUTH DUPONT HIGHWAY Dover, DE 19901 |
Product Code | KKX |
CFR Regulation Number | 878.4370 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-09-30 |
Decision Date | 2015-06-24 |