Inflate-A-Cuff #7014

FDA 510(k) K910903 · Pa Medical Corp.

Substantially Equivalent

510(k) numberK910903

Submission

Device name
Inflate-A-Cuff #7014
Applicant
Pa Medical Corp.
Columbia, TN, US
Received
March 5, 1991
Decision date
May 8, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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More from Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

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Questions and answers

When was Inflate-A-Cuff #7014 cleared by the FDA?

Inflate-A-Cuff #7014 (K910903) received a 510(k) decision of Substantially Equivalent on May 8, 1991, 64 days after the submission was received.

What is the product code of K910903?

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