T-Vac Pleural Drainage Unit, 7800 Series

FDA 510(k) K861025 · Boehringer Laboratories

Substantially Equivalent

510(k) numberK861025

Submission

Device name
T-Vac Pleural Drainage Unit, 7800 Series
Applicant
Boehringer Laboratories
Norristown, PA, US
Received
March 18, 1986
Decision date
April 28, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KDQ – Bottle, Collection, Vacuum
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6740
Specialty
General Hospital

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Questions and answers

When was T-Vac Pleural Drainage Unit, 7800 Series cleared by the FDA?

T-Vac Pleural Drainage Unit, 7800 Series (K861025) received a 510(k) decision of Substantially Equivalent on April 28, 1986, 41 days after the submission was received.

What is the product code of K861025?

The FDA product code is KDQ – Bottle, Collection, Vacuum, a Class II (moderate risk) device regulated under 21 CFR 880.6740.