GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER— 510(k) K850260

Name: FDA 510(k) clearance K850260
Creator: U.S. Food and Drug Administration
Published: 1985-02-27

Substantially Equivalent

Gelman Sciences, Inc.

FDA 510(k) clearance K850260 for GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER, Substantially Equivalent on 1985-02-27. Applicant: Gelman Sciences, Inc.. Device class: 1.

Clearance details

Applicant: Gelman Sciences, Inc.
Product code: Code JQT
Device class: Class 1
Regulation: 21 CFR 862.2400
Advisory panel: Clinical Chemistry
Date received: 1985-01-22
Decision date: 1985-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ann Arbor, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JQT

view all

K111356 — ASIMANAGER - AT2011-11-09
K944185 — ISOSCAN1994-11-17
K915332 — MODEL 795 FLUOROMETER/DENSITOMETER1992-02-18
K885254 — TARGET READER1989-01-27
K860645 — ELECTROPHORESIS DATA CENTER (EDC)1986-12-17

More clearances from Gelman Sciences, Inc.

view all

K946190 — DRUG DISPENSING SPIKE1995-03-17
K943127 — PHARMASSURE LARGE VOLUME TRANSFER FILTERS1994-09-29
K941589 — SYRINGE FILTER DEVICES1994-09-06
K941020 — DRUG RECONSTITUTION FILTER DEVICE1994-08-10
K942275 — VIAL VENT FILTER1994-07-26

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