Model RCV Reflux Check Valve

FDA 510(k) K862327 · Life-Tech Intl., Inc.

Substantially Equivalent

510(k) numberK862327

Submission

Device name
Model RCV Reflux Check Valve
Applicant
Life-Tech Intl., Inc.
Houston, TX, US
Received
June 19, 1986
Decision date
September 4, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FAP – Cystometric Gas (Carbon-Dioxide) On Hydraulic Device
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1620
Specialty
Gastroenterology, Urology

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K946108Ear-A-GatorKHH · Traditional 06/13/1995SE
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Questions and answers

When was Model RCV Reflux Check Valve cleared by the FDA?

Model RCV Reflux Check Valve (K862327) received a 510(k) decision of Substantially Equivalent on September 4, 1986, 77 days after the submission was received.

What is the product code of K862327?

The FDA product code is FAP – Cystometric Gas (Carbon-Dioxide) On Hydraulic Device, a Class II (moderate risk) device regulated under 21 CFR 876.1620.