The following data is part of a premarket notification filed by Arista Latindo Industrial, Ltd. P.t. with the FDA for Powder Free Synthetic Examination Gloves.
Device ID | K971356 |
510k Number | K971356 |
Device Name: | POWDER FREE SYNTHETIC EXAMINATION GLOVES |
Classification | Polymer Patient Examination Glove |
Applicant | ARISTA LATINDO INDUSTRIAL, LTD. P.T. 128 JALAN KYAI HAJI MUHAMMAD MANSYUR Jakarta Barat, ID 11210 |
Contact | Linga Sumarta |
Correspondent | Linga Sumarta ARISTA LATINDO INDUSTRIAL, LTD. P.T. 128 JALAN KYAI HAJI MUHAMMAD MANSYUR Jakarta Barat, ID 11210 |
Product Code | LZA |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-04-11 |
Decision Date | 1997-09-05 |