Scimed R30 Silicone Assist Reservoir

FDA 510(k) K882720 · Scimed Life Systems, Inc.

Substantially Equivalent

510(k) numberK882720

Submission

Device name
Scimed R30 Silicone Assist Reservoir
Applicant
Scimed Life Systems, Inc.
Minneapolis, MN, US
Received
July 1, 1988
Decision date
September 16, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DTN – Reservoir, Blood, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4400
Specialty
Cardiovascular

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Questions and answers

When was Scimed R30 Silicone Assist Reservoir cleared by the FDA?

Scimed R30 Silicone Assist Reservoir (K882720) received a 510(k) decision of Substantially Equivalent on September 16, 1988, 77 days after the submission was received.

What is the product code of K882720?

The FDA product code is DTN – Reservoir, Blood, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4400.