Kendall SCD 700 Sequential Compression Controller

FDA 510(k) K132360 · Covidien

Substantially Equivalent

510(k) numberK132360

Submission

Device name
Kendall SCD 700 Sequential Compression Controller
Applicant
Covidien
Mansfield, MA, US
Received
July 30, 2013
Decision date
August 27, 2013
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOW – Sleeve, Limb, Compressible
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5800
Specialty
Cardiovascular

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Questions and answers

When was Kendall SCD 700 Sequential Compression Controller cleared by the FDA?

Kendall SCD 700 Sequential Compression Controller (K132360) received a 510(k) decision of Substantially Equivalent on August 27, 2013, 28 days after the submission was received.

What is the product code of K132360?

The FDA product code is JOW – Sleeve, Limb, Compressible, a Class II (moderate risk) device regulated under 21 CFR 870.5800.