Cleared Traditional

K792108 - CONPHAR BLOOD PRESSURE CUFFS

K792108 is an FDA 510(k) clearance for CONPHAR BLOOD PRESSURE CUFFS, manufactured by Conphar, Inc.. The device is a Class 2 Cardiovascular device with product code DXQ cleared through the Traditional 510(k) pathway after a 40-day FDA review.

K792108 · Conphar, Inc. · Cardiovascular device
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Dec 1979
Decision
40d
Days
Class 2
Risk

K792108 is an FDA 510(k) clearance for the CONPHAR BLOOD PRESSURE CUFFS. Classified as Blood Pressure Cuff (product code DXQ), Class II - Special Controls.

Submitted by Conphar, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 4, 1979 after a review of 40 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1120 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Conphar, Inc. devices

FDA 510(k) Submission Details - K792108

510(k) Number K792108 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 25, 1979
Decision Date December 04, 1979
Days to Decision 40 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 125d · This submission: 40d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DXQ Device Classification - Class 2, Special Controls

Product Code DXQ Blood Pressure Cuff
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1120
Definition 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.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DXQ Blood Pressure Cuff

All 87
Devices cleared under the same product code (DXQ) and FDA review panel - the closest regulatory comparables to K792108.
CONPHAR WALL MODEL MERCURY SPHYGMOMAN.
K801182 · Conphar, Inc. · Jun 1980
ABCO MERCURIAL SPHYGMOMANOMETER
K800236 · Abco Dealers, Inc. · Feb 1980
ANEROID SPHYMOMANOMETER
K792355 · Abco Dealers, Inc. · Dec 1979
PARKE-DAVIS TOTAL HIP PROSTHESIS
K791875 · Warner-Lambert Co. · Oct 1979
ANEROID SPHYGMOMANOMETER
K760655 · Abco Dealers, Inc. · Oct 1976