X-Coated Capiox SX18 and SX25 Hollow Fiber Oxygenator With/ Without Detachable Hardshell Reservoir

FDA 510(k) K993772 · Terumo Medical Corp.

Substantially Equivalent

510(k) numberK993772

Submission

Device name
X-Coated Capiox SX18 and SX25 Hollow Fiber Oxygenator With/ Without Detachable Hardshell Reservoir
Applicant
Terumo Medical Corp.
Elkton, MD, US
Received
November 8, 1999
Decision date
June 5, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DTZ – Oxygenator, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4350
Specialty
Cardiovascular
Life-sustaining
Yes

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Questions and answers

When was X-Coated Capiox SX18 and SX25 Hollow Fiber Oxygenator With/ Without Detachable Hardshell Reservoir cleared by the FDA?

X-Coated Capiox SX18 and SX25 Hollow Fiber Oxygenator With/ Without Detachable Hardshell Reservoir (K993772) received a 510(k) decision of Substantially Equivalent on June 5, 2000, 210 days after the submission was received.

What is the product code of K993772?

The FDA product code is DTZ – Oxygenator, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4350.