DATA MODULE— 510(k) K781915

Substantially Equivalent

Waters Assoc., Inc.

FDA 510(k) clearance K781915 for DATA MODULE, Substantially Equivalent on 1979-01-10. Applicant: Waters Assoc., Inc.. Device class: 1.

Clearance details

Applicant: Waters Assoc., Inc.
Product code: Code KIE
Device class: Class 1
Regulation: 21 CFR 862.2260
Advisory panel: Clinical Chemistry
Date received: 1978-11-14
Decision date: 1979-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K911299 — EQUIPMENT/MATERIAL DECONTAMINATING KIT1991-04-08

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K801852 — MRM-2 OXYGEN CONSUMPTION MONITOR1980-08-20
K801431 — PAN-AM MYELOGRAM TRAY1980-08-12
K791661 — SYSTEM CONTROLLER 720 SERIES1979-09-24

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