CALIBRATOR, DYNAMIC— 510(k) K781692

Substantially Equivalent

Waters Assoc., Inc.

FDA 510(k) clearance K781692 for CALIBRATOR, DYNAMIC, Substantially Equivalent on 1978-11-29. Applicant: Waters Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Waters Assoc., Inc.
Product code: Code DXM
Device class: Class 2
Regulation: 21 CFR 870.1450
Advisory panel: Cardiovascular
Date received: 1978-10-04
Decision date: 1978-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DXM

K791892 — TAPE-A-TRACE1979-11-05

More clearances from Waters Assoc., Inc.

K811975 — MODEL 480 VARIABLE WAVELENGTH ULTRA VIOL1981-07-27
K802481 — 7FRENCH FLOW DIRECTED TRIPLE LUMEN CATH1980-10-31
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.