POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE

FDA 510(k) Premarket Notification · Submission K101595 · Applicant: Better Care Plastic Technology Cp., Ltd.

Public Record 510(k) Submission Decision Date: 2010-08-06 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K101595.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K101595
Device Name
POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE
Product Code
LZA
Decision Date
2010-08-06
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General Hospital (HO)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2010-06-08

Related Establishments / Registrations

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