Cleared Traditional

K813174 - BRADYCARDIA ALARM

K813174 is an FDA 510(k) clearance for BRADYCARDIA ALARM, manufactured by Douglas Scientific Products. The device is a Class 2 Cardiovascular device with product code DRT cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K813174 · Douglas Scientific Products · Cardiovascular device
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Jan 1982
Decision
77d
Days
Class 2
Risk

K813174 is an FDA 510(k) clearance for the BRADYCARDIA ALARM. Classified as Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) (product code DRT), Class II - Special Controls.

Submitted by Douglas Scientific Products (Mchenry, US). The FDA issued a Cleared decision on January 22, 1982 after a review of 77 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2300 - 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 Douglas Scientific Products devices

FDA 510(k) Submission Details - K813174

510(k) Number K813174 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 06, 1981
Decision Date January 22, 1982
Days to Decision 77 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
48d faster than avg
Panel avg: 125d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DRT Device Classification - Class 2, Special Controls

Product Code DRT Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2300
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 - DRT Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm)

All 229
Devices cleared under the same product code (DRT) and FDA review panel - the closest regulatory comparables to K813174.
#505 PORT. VITAL FUNCTIONS NEONATAL MON
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#506 PORT. VITAL FUNCTIONS NEONATAL MON
K820417 · Ge Medical Systems Information Technologies · Mar 1982
SYSTEM V.HEART RATE/RESPIR. RATE MONIT.
K820114 · Narco Air-Shields · Feb 1982
NIHON KOHDEN HEART MONITORS OMP 7101-02
K813444 · Nihon Kohden America, Inc. · Dec 1981
MODEL 2000 MONITOR
K812828 · Datascope Corp. · Nov 1981
INFANT CARIDAC MONITOR
K812674 · Electromed Intl., Ltd. · Oct 1981