C-Flo Suction Tube

FDA 510(k) K882121 · Concept, Inc.

Substantially Equivalent

510(k) numberK882121

Submission

Device name
C-Flo Suction Tube
Applicant
Concept, Inc.
Clearwater, FL, US
Received
May 19, 1988
Decision date
June 20, 1988
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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K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)DXQ · Special Unimed Medical Supplies, Inc.01/09/2026SE
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Questions and answers

When was C-Flo Suction Tube cleared by the FDA?

C-Flo Suction Tube (K882121) received a 510(k) decision of Substantially Equivalent on June 20, 1988, 32 days after the submission was received.

What is the product code of K882121?

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