Devon Accubp Cuff

FDA 510(k) K090664 · Devon Medical, Inc.

Substantially Equivalent

510(k) numberK090664

Submission

Device name
Devon Accubp Cuff
Applicant
Devon Medical, Inc.
King Of Prussia, PA, US
Received
March 13, 2009
Decision date
March 23, 2009
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
DXQ – Blood Pressure Cuff
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1120
Specialty
Cardiovascular

A blood pressure cuff is a device that has an inflatable bladder in an elastic sleeve (cuff) with a mechanism for inflating the bladder. The cuff is used to determine a subject's blood pressure.

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Questions and answers

When was Devon Accubp Cuff cleared by the FDA?

Devon Accubp Cuff (K090664) received a 510(k) decision of Substantially Equivalent on March 23, 2009, 10 days after the submission was received.

What is the product code of K090664?

The FDA product code is DXQ – Blood Pressure Cuff, a Class II (moderate risk) device regulated under 21 CFR 870.1120.