STERILE & NON-STERILE SURGEONS GLOVES— 510(k) K882200

Name: FDA 510(k) clearance K882200
Creator: U.S. Food and Drug Administration
Published: 1989-02-03

Substantially Equivalent

Taroko Ent., Ltd.

FDA 510(k) clearance K882200 for STERILE & NON-STERILE SURGEONS GLOVES, Substantially Equivalent on 1989-02-03. Applicant: Taroko Ent., Ltd.. Device class: 1.

Clearance details

Applicant: Taroko Ent., Ltd.
Product code: Code KGO
Device class: Class 1
Regulation: 21 CFR 878.4460
Advisory panel: General, Plastic Surgery
Date received: 1988-05-16
Decision date: 1989-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, 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.