Conphar Wall Model Mercury Sphygmoman.

FDA 510(k) K801182 · Conphar, Inc.

Substantially Equivalent

510(k) numberK801182

Submission

Device name
Conphar Wall Model Mercury Sphygmoman.
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
May 16, 1980
Decision date
June 4, 1980
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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Questions and answers

When was Conphar Wall Model Mercury Sphygmoman. cleared by the FDA?

Conphar Wall Model Mercury Sphygmoman. (K801182) received a 510(k) decision of Substantially Equivalent on June 4, 1980, 19 days after the submission was received.

What is the product code of K801182?

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