NITRILE PATIENT EXAMINATION GLOVE, BLUE OR GREEN COLORED (PREPOWDERED USP)— 510(k) K984356

Substantially Equivalent

Perusahaan Getah Asas Sdn. Bhd.

FDA 510(k) clearance K984356 for NITRILE PATIENT EXAMINATION GLOVE, BLUE OR GREEN COLORED (PREPOWDERED USP), Substantially Equivalent on 1999-01-08. Applicant: Perusahaan Getah Asas Sdn. Bhd.. Device class: 1.

Clearance details

Applicant
Perusahaan Getah Asas Sdn. Bhd.
Product code
Code LZA
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Selangor, Darul Ehsan, MY
Download summary PDFView on FDA.gov ↗

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Adverse events under product code LZA

product code LZA
Other
1
Total
1

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.