NEOTECH UNIVERSAL ADAPTER— 510(k) K882203

Name: FDA 510(k) clearance K882203
Creator: U.S. Food and Drug Administration
Published: 1988-06-17

Substantially Equivalent

Neotech Products, Inc.

FDA 510(k) clearance K882203 for NEOTECH UNIVERSAL ADAPTER, Substantially Equivalent on 1988-06-17. Applicant: Neotech Products, Inc.. Device class: 1.

Clearance details

Applicant: Neotech Products, Inc.
Product code: Code BZA
Device class: Class 1
Regulation: 21 CFR 868.5810
Advisory panel: Anesthesiology
Date received: 1988-05-25
Decision date: 1988-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chatsworth, CA, 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.