Latex Penrose Drain Tubing

FDA 510(k) K821700 · Abco Dealers, Inc.

Substantially Equivalent

510(k) numberK821700

Submission

Device name
Latex Penrose Drain Tubing
Applicant
Abco Dealers, Inc.
Mchenry, IL, US
Received
June 8, 1982
Decision date
June 16, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GAX – Tourniquet, Nonpneumatic
Device class
Class I (low risk)
Regulation
21 CFR 878.5900
Specialty
General, Plastic Surgery

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Questions and answers

When was Latex Penrose Drain Tubing cleared by the FDA?

Latex Penrose Drain Tubing (K821700) received a 510(k) decision of Substantially Equivalent on June 16, 1982, 8 days after the submission was received.

What is the product code of K821700?

The FDA product code is GAX – Tourniquet, Nonpneumatic, a Class I (low risk) device regulated under 21 CFR 878.5900.