LATEX SURGICAL GLOVE (NON STERILE)— 510(k) K883556

Name: FDA 510(k) clearance K883556
Creator: U.S. Food and Drug Administration
Published: 1989-02-03

Substantially Equivalent

Makintech Corp.

FDA 510(k) clearance K883556 for LATEX SURGICAL GLOVE (NON STERILE), Substantially Equivalent on 1989-02-03. Applicant: Makintech Corp.. Device class: 1.

Clearance details

Applicant: Makintech Corp.
Product code: Code KGO
Device class: Class 1
Regulation: 21 CFR 878.4460
Advisory panel: General, Plastic Surgery
Date received: 1988-08-19
Decision date: 1989-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cleveland, OH, US

Download summary PDF View on FDA.gov ↗

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