Linear Cloud Tonometer

FDA 510(k) K841089 · Linear Tonometers, Inc.

Substantially Equivalent

510(k) numberK841089

Submission

Device name
Linear Cloud Tonometer
Applicant
Linear Tonometers, Inc.
Mchenry, IL, US
Received
March 13, 1984
Decision date
May 22, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LCH – Tonometer (Calibration And Q.C. Of Blood-Gas Instruments), Clinical
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

Other 510(k)s with product code LCH

510(k)DeviceApplicantDecision
K922386RNA Medical TonometerLCH · Traditional Bionostics, Inc.06/26/1992SE
K904163Clinical Blood Gas MixturesLCH · Traditional Norco, Inc.11/01/1990SE
K900819Blood Gas Calibration StandardLCH · Traditional Cryogenic Rare Gas Laboratories, Inc.04/25/1990SE
K862958Amr Research TonometerLCH · Traditional Associated Medical Representatives11/24/1986SE
K802379Hem-O-Scan Oxygen Equil. Curve AnalyzerLCH · Traditional American Instrument Co.10/31/1980SE
K801599Corning 184 Blood Gas TonometerLCH · Traditional Corning Medical & Scientific08/20/1980SE
K781417Precision Gas MixerLCH · Traditional Medicor USA , Ltd.09/20/1978SE
K781386Ebs 775 TonometerLCH · Traditional Equilibrated Bio Systems, Inc.09/14/1978SE

Questions and answers

When was Linear Cloud Tonometer cleared by the FDA?

Linear Cloud Tonometer (K841089) received a 510(k) decision of Substantially Equivalent on May 22, 1984, 70 days after the submission was received.

What is the product code of K841089?

The FDA product code is LCH – Tonometer (Calibration And Q.C. Of Blood-Gas Instruments), Clinical, a Class I (low risk) device regulated under 21 CFR 862.1660.