Cleared Traditional

K884405 - FORTEC MI-150 DIGITAL BLOOD PRESSURE METER

K884405 is an FDA 510(k) clearance for FORTEC MI-150 DIGITAL BLOOD PRESSURE METER, manufactured by Nam Tai Electronic & Electrical Products, Ltd.. The device is a Class 2 Cardiovascular device with product code DXN cleared through the Traditional 510(k) pathway after a 211-day FDA review.

K884405 · Nam Tai Electronic & Electrical Products, Ltd. · Cardiovascular device
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May 1989
Decision
211d
Days
Class 2
Risk

K884405 is an FDA 510(k) clearance for the FORTEC MI-150 DIGITAL BLOOD PRESSURE METER. Classified as System, Measurement, Blood-pressure, Non-invasive (product code DXN), Class II - Special Controls.

Submitted by Nam Tai Electronic & Electrical Products, Ltd. (Kowloon, Hong Kong, HK). The FDA issued a Cleared decision on May 19, 1989 after a review of 211 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Nam Tai Electronic & Electrical Products, Ltd. devices

FDA 510(k) Submission Details - K884405

510(k) Number K884405 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 20, 1988
Decision Date May 19, 1989
Days to Decision 211 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
86d slower than avg
Panel avg: 125d · This submission: 211d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DXN Device Classification - Class 2, Special Controls

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 917
Devices cleared under the same product code (DXN) and FDA review panel - the closest regulatory comparables to K884405.
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K882824 · A&D Engineering, Inc. · Jan 1989