H-RAY

Vinyl Patient Examination Glove

SHIJIAZHUANG HONGRAY PLASTIC PRODUCTS CO., LTD.

The following data is part of a premarket notification filed by Shijiazhuang Hongray Plastic Products Co., Ltd. with the FDA for H-ray.

Pre-market Notification Details

Device IDK982720
510k NumberK982720
Device Name:H-RAY
ClassificationVinyl Patient Examination Glove
Applicant SHIJIAZHUANG HONGRAY PLASTIC PRODUCTS CO., LTD. NO. 135 XIN-HUA WEST RD. Shijiazhuang,  CN 050081
ContactLin Chin Yu
CorrespondentLin Chin Yu
SHIJIAZHUANG HONGRAY PLASTIC PRODUCTS CO., LTD. NO. 135 XIN-HUA WEST RD. Shijiazhuang,  CN 050081
Product CodeLYZ  
CFR Regulation Number880.6250 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1998-08-04
Decision Date1998-11-05
Summary:summary

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