VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)— 510(k) K890968

Name: FDA 510(k) clearance K890968
Creator: U.S. Food and Drug Administration
Published: 1989-07-31

Substantially Equivalent

Interpro Intl., Inc.

FDA 510(k) clearance K890968 for VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX), Substantially Equivalent on 1989-07-31. Applicant: Interpro Intl., Inc.. Device class: 1.

Clearance details

Applicant: Interpro Intl., Inc.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-02-27
Decision date: 1989-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerville, NJ, US

Download summary PDF View on FDA.gov ↗

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K891438 — PATIENT EXAMINATION GLOVES (LATEX)1989-05-31
K891440 — PATIENT EXAMINATION GLOVES (LATEX)1989-05-31
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Data sourced from openFDA. This site is unofficial and independent of the FDA.