Mini-Chem Analyzer

FDA 510(k) K860987 · Ocean Scientific, Inc.

Substantially Equivalent

510(k) numberK860987

Submission

Device name
Mini-Chem Analyzer
Applicant
Ocean Scientific, Inc.
Garden Grove, CA, US
Received
March 17, 1986
Decision date
May 5, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJQ – Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2300
Specialty
Clinical Chemistry

Other 510(k)s with product code JJQ

510(k)DeviceApplicantDecision
K013371UBIT-IR300 Infrared Spectrometry SystemJJQ · Traditional Otsuka Pharmaceutical Co., Ltd.12/21/2001SE
K980120Digene DML 2000 Microplate LuminometerJJQ · Traditional Digene Corp.02/06/1998SE
K973938Alpha 4 LS Automated Microtiterplate Processor and ReaderJJQ · Traditional Sfri, Inc.02/04/1998SE
K974762Stat TracksJJQ · Traditional Awareness Technology, Inc.01/28/1998SE
K962113Anthos Phacts Version Microplate ReaderJJQ · Traditional Columbia Bioscience, Inc.11/05/1996SE
K961183Cbi 7520 ReaderJJQ · Traditional Columbia Bioscience, Inc.08/02/1996SE
K962166Origen AnalyzerJJQ · Traditional Igen, Inc.07/31/1996SE
K955077Anthos 2010 ReaderJJQ · Traditional Anthos Labtec, Inc.12/04/1995SE
K953710ELX808 Automated Microplate ReadersJJQ · Traditional Bio-Tek Instruments, Inc.10/25/1995SE
K953572ELX800UVJJQ · Traditional Bio-Tek Instruments, Inc.10/19/1995SE

More from Bio-Tek Instruments, Inc.

510(k)DeviceDecision
K893810Immuno-Wash Automated Tube WasherJQW · Traditional 08/03/1989SE
K873638Micro-Chem AnalyzerJJQ · Traditional 09/29/1987SE
K864731Ocean Scientific VDRL TestGMQ · Traditional 03/10/1987SE
K863976Ocean Scientific VacutestJKA · Traditional 10/24/1986SE
K840340Chem-Stat AnalyzerJJQ · Traditional 03/23/1984SE

Questions and answers

When was Mini-Chem Analyzer cleared by the FDA?

Mini-Chem Analyzer (K860987) received a 510(k) decision of Substantially Equivalent on May 5, 1986, 49 days after the submission was received.

What is the product code of K860987?

The FDA product code is JJQ – Colorimeter, Photometer, Spectrophotometer For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2300.