The following data is part of a premarket notification filed by Purnabina Sdn Bhd with the FDA for Patient Examination Gloves (latex).
Device ID | K891507 |
510k Number | K891507 |
Device Name: | PATIENT EXAMINATION GLOVES (LATEX) |
Classification | Latex Patient Examination Glove |
Applicant | PURNABINA SDN BHD 7.5KM JALAN MERSING KLUANG INDUSTRIAL AREA, KLUANG Johor, MY 86000 |
Contact | Siew Hock |
Correspondent | Siew Hock PURNABINA SDN BHD 7.5KM JALAN MERSING KLUANG INDUSTRIAL AREA, KLUANG Johor, MY 86000 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-03-16 |
Decision Date | 1989-04-06 |