The following data is part of a premarket notification filed by Shield Gloves Manufacturer (m) Sdn Bhd with the FDA for Royal Shield Non-sterile Powdered Latex Examination Gloves (protein Labeling Claim) 200 Mcgm Or Less Of Total Water Extr.
Device ID | K992417 |
510k Number | K992417 |
Device Name: | ROYAL SHIELD NON-STERILE POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABELING CLAIM) 200 MCGM OR LESS OF TOTAL WATER EXTR |
Classification | Latex Patient Examination Glove |
Applicant | SHIELD GLOVES MANUFACTURER (M) SDN BHD P.O. BOX 4341 Crofton, MD 21114 |
Contact | E.j. Smith |
Correspondent | E.j. Smith SHIELD GLOVES MANUFACTURER (M) SDN BHD P.O. BOX 4341 Crofton, MD 21114 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-07-20 |
Decision Date | 1999-09-13 |
Summary: | summary |