Cleared Traditional

K780598 - TREND II ANEROID

K780598 is the FDA 510(k) clearance for TREND II ANEROID by Abco Dealers, Inc.. It is a Class 2 Cardiovascular device (product code DXN) cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K780598 · Abco Dealers, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1978
Decision
57d
Days
Class 2
Risk

K780598 is an FDA 510(k) clearance for the TREND II ANEROID. Classified as System, Measurement, Blood-pressure, Non-invasive (product code DXN), Class II - Special Controls.

Submitted by Abco Dealers, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 6, 1978 after a review of 57 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 Abco Dealers, Inc. devices

Submission Details

510(k) Number K780598 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 10, 1978
Decision Date June 06, 1978
Days to Decision 57 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
68d faster than avg
Panel avg: 125d · This submission: 57d
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 516
Devices cleared under the same product code (DXN) and FDA review panel - the closest regulatory comparables to K780598.
QUICK-CHECK
K790277 · United States Surgical, A Division of Tyco Healthc · Mar 1979
AUTOMATIC BLOOD PRESSURE DEVICE
K781517 · Welch Allyn, Inc. · Jan 1979
PRESSURE INFUSION CUFF
K781556 · Abbott Laboratories · Oct 1978
ELHCTRONIC SPHYGMOMANOMETER
K771393 · C.R. Bard, Inc. · Nov 1977
ELECTRONIC STETHESCOPE
K771394 · C.R. Bard, Inc. · Nov 1977
PRESSUROMETER II
K771500 · Del Mar Avionics · Aug 1977