NEOLINE(TM)— 510(k) K914778

Unknown

Martech Medical Products, Inc.

FDA 510(k) clearance K914778 for NEOLINE(TM), Unknown on 1992-09-16. Applicant: Martech Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Martech Medical Products, Inc.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1991-10-23
Decision date: 1992-09-16
Decision: Unknown
Clearance type: Traditional
Location: Temecula, 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.