Cry-Actrackercam

FDA 510(k) K110305 · Brymill Cryogenic Cystems

Substantially Equivalent

510(k) numberK110305

Submission

Device name
Cry-Actrackercam
Applicant
Brymill Cryogenic Cystems
Ellington, CT, US
Received
February 2, 2011
Decision date
January 13, 2012
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FQZ – Thermometer, Clinical Color Change
Device class
Class I (low risk)
Regulation
21 CFR 880.2900
Specialty
General Hospital

Other 510(k)s with product code FQZ

510(k)DeviceApplicantDecision
K963049Steri-Aid KitFQZ · Traditional Steri-Aid, Inc.11/12/1996SE
K946046Deroyal Technologices, Inc. Liquid Crystal Skin Temperature StripFQZ · Traditional Deroyal Critical Care, Div. Deroyal Technologies07/19/1995SE
K894893Point Checker Color Strip ThermometerFQZ · Traditional Kyowa Medex Co., Ltd.04/05/1990SE
K884612Franklin Collector(R)FQZ · Traditional Franklin Diagnostics, Inc.03/27/1989SE
K881286Tempa-Dot Clinical Thermometer SheathFQZ · Traditional Pymah Corp.06/08/1988SE
K863181Healthcheck Therm-StripFQZ · Traditional Healthcheck Corp.09/11/1986SE
K853515Pee Wee ThermometersFQZ · Traditional Joel R.L. Ehren Kranz10/16/1985SE
K822423Baby Temp PacifierFQZ · Traditional Trp Energy Sensors, Inc.10/13/1982SE
K791574Modified Tempa-Dot ThermometerFQZ · Traditional Info-Chem09/12/1979SE
K790890TEMPO2-I Disposable ThermometersFQZ · Traditional Airlife, Inc.06/27/1979SE

Questions and answers

When was Cry-Actrackercam cleared by the FDA?

Cry-Actrackercam (K110305) received a 510(k) decision of Substantially Equivalent on January 13, 2012, 345 days after the submission was received.

What is the product code of K110305?

The FDA product code is FQZ – Thermometer, Clinical Color Change, a Class I (low risk) device regulated under 21 CFR 880.2900.