FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇳 China

Nitrile Patient Examination Glove

K Number: K210723 · Decision Jul 12, 2021
Classifications
1
FEI Numbers
380
Registration Numbers
380
Same Product Code
1171
Applicant Total
2
Review Days
124

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Basic Information

Device Name
Nitrile Patient Examination Glove
K Number
K210723
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jiangxi Zhonghong Pulin Medical Products Co., Ltd.
Date Received
March 10, 2021
Decision Date
July 12, 2021
Product Code
LZA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LZA Polymer Patient Examination Glove

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LZA), ordered by most recent decision date.

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Other Clearances by Jiangxi Zhonghong Pulin Medical Products Co., Ltd.

K Number Device Name
K182117 Vinyl Patient Examination Gloves