ULTRASCAN CLINICAL ANALYZER— 510(k) K862999

Name: FDA 510(k) clearance K862999
Creator: U.S. Food and Drug Administration
Published: 1986-09-15

Substantially Equivalent

Specialty Medical Industries, Inc.

FDA 510(k) clearance K862999 for ULTRASCAN CLINICAL ANALYZER, Substantially Equivalent on 1986-09-15. Applicant: Specialty Medical Industries, Inc.. Device class: 1.

Clearance details

Applicant: Specialty Medical Industries, Inc.
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1986-08-08
Decision date: 1986-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JJQ

view all

K013371 — UBIT-IR300 INFRARED SPECTROMETRY SYSTEM2001-12-21
K980120 — DIGENE DML 2000 MICROPLATE LUMINOMETER1998-02-06
K973938 — ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER1998-02-04
K974762 — STAT TRACKS1998-01-28
K962113 — ANTHOS PHACTS VERSION MICROPLATE READER1996-11-05

More clearances from Specialty Medical Industries, Inc.

view all

K872968 — ULTRASCAN IGE ASSAY KIT1987-08-28
K790808 — PROTEIN ASSAY KIT1979-11-05

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