Cleared Traditional

K863672 - MODEL (MB-700) BLOOD PRESSURE MONITOR

K863672 is the FDA 510(k) clearance for MODEL (MB-700) BLOOD PRESSURE MONITOR by Sharp Electronics Corp.. It is a Class 2 Cardiovascular device (product code DXN) cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K863672 · Sharp Electronics Corp. · Cardiovascular device
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Nov 1986
Decision
76d
Days
Class 2
Risk

K863672 is an FDA 510(k) clearance for the MODEL (MB-700) BLOOD PRESSURE MONITOR. Classified as System, Measurement, Blood-pressure, Non-invasive (product code DXN), Class II - Special Controls.

Submitted by Sharp Electronics Corp. (Mahwah, US). The FDA issued a Cleared decision on November 18, 1986 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1130 - 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 Sharp Electronics Corp. devices

Submission Details

510(k) Number K863672 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 03, 1986
Decision Date November 18, 1986
Days to Decision 76 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 125d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DXN System, Measurement, Blood-pressure, Non-invasive
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1130
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 - DXN System, Measurement, Blood-pressure, Non-invasive

All 529
Devices cleared under the same product code (DXN) and FDA review panel - the closest regulatory comparables to K863672.
NBP 488, TPR 488
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K861504 · Fukuda Denshi USA, Inc. · Aug 1986
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K855127 · Spacelabs, Inc. · Aug 1986
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K853561 · Physio-Control Corp. · Jun 1986