ELECTRA AUTOMATIC SAMPLER— 510(k) K864875

Name: FDA 510(k) clearance K864875
Creator: U.S. Food and Drug Administration
Published: 1987-02-13

Substantially Equivalent

Medical Laboratory Automation Systems, Inc.

FDA 510(k) clearance K864875 for ELECTRA AUTOMATIC SAMPLER, Substantially Equivalent on 1987-02-13. Applicant: Medical Laboratory Automation Systems, Inc.. Device class: 1.

Clearance details

Applicant: Medical Laboratory Automation Systems, Inc.
Product code: Code JQW
Device class: Class 1
Regulation: 21 CFR 862.2750
Advisory panel: Clinical Chemistry
Date received: 1986-12-12
Decision date: 1987-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasantville, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JQW

view all

K023955 — BD VIPER INSTRUMENT2003-06-24
K973335 — QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)1998-04-30
K980180 — 2700 SAMPLE MANAGER1998-02-12
K970420 — MASTERCAP AM 5.0/MASTERCAP RM 5.01997-06-30
K970616 — MINI SAMPLER PROCESSOR1997-04-21

More clearances from Medical Laboratory Automation Systems, Inc.

view all

K962664 — ELECTRA 1800C AUTOMATIC COAGULATION ANALYZER1996-09-10
K944227 — ELECTRA 1400C AUTOMATIC COAGULATION ANALYZER1995-02-03
K931206 — ELECTRA 1600C AUTOMATIC COAGULATION TIMER1993-08-23
K923220 — THROMBIN CLOT TIME TEST PROCEDURE1992-09-29
K903638 — GASTRO-INTESTINAL ACCU-CULSHURE TM1991-01-18

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