Sci Med Tubing Connectors

FDA 510(k) K831261 · Scimed Life Systems, Inc.

Substantially Equivalent

510(k) numberK831261

Submission

Device name
Sci Med Tubing Connectors
Applicant
Scimed Life Systems, Inc.
Mchenry, IL, US
Received
April 18, 1983
Decision date
June 3, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DTL – Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4290
Specialty
Cardiovascular

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Questions and answers

When was Sci Med Tubing Connectors cleared by the FDA?

Sci Med Tubing Connectors (K831261) received a 510(k) decision of Substantially Equivalent on June 3, 1983, 46 days after the submission was received.

What is the product code of K831261?

The FDA product code is DTL – Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4290.