The following data is part of a premarket notification filed by Shanghai Pt Plastics Enterprise Company, Ltd. with the FDA for Patient Examination Glove.
Device ID | K961521 |
510k Number | K961521 |
Device Name: | PATIENT EXAMINATION GLOVE |
Classification | Vinyl Patient Examination Glove |
Applicant | SHANGHAI PT PLASTICS ENTERPRISE COMPANY, LTD. NO. 268, YUSHU ROAD CANGQIAO TOWNSHIP Songjiang County Shanghai, CN |
Contact | Peter Wang |
Correspondent | Peter Wang SHANGHAI PT PLASTICS ENTERPRISE COMPANY, LTD. NO. 268, YUSHU ROAD CANGQIAO TOWNSHIP Songjiang County Shanghai, CN |
Product Code | LYZ |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-04-22 |
Decision Date | 1997-01-30 |