Bili-Meter

FDA 510(k) K953005 · Olympic Medical Corp.

Substantially Equivalent

510(k) numberK953005

Submission

Device name
Bili-Meter
Applicant
Olympic Medical Corp.
Seattle, WA, US
Received
June 28, 1995
Decision date
September 28, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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

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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
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K020335Olympic Medical Lectromed Cerebral Function Monitor System, Model 5330OMC · Traditional 06/18/2002SE
K001056Olympic Warm-UpILY · Traditional 09/29/2000SE
K983229Olympic Medical Lectromed Cerebral Function Monitor SystemOMA · Traditional 03/23/1999SE
K971601Olympic Bili-BassinetLBI · Traditional 09/24/1997SE
K972193Olympix Mini-Pasteurmatic (58210)LDS · Traditional 09/05/1997SE
K971117WarmetteLHC · Traditional 08/22/1997SE
K955357Olympic Smart Scale Model 50/50RAFRW · Traditional 01/30/1996SE
K954434Olympic Infant ThermometerFLL · Traditional 12/20/1995SE

Questions and answers

When was Bili-Meter cleared by the FDA?

Bili-Meter (K953005) received a 510(k) decision of Substantially Equivalent on September 28, 1995, 92 days after the submission was received.

What is the product code of K953005?

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