Cleared Traditional

K970603 - D SERIES ELECTRODE

K970603 is an FDA 510(k) clearance for D SERIES ELECTRODE, manufactured by Cmc Sense-It, Inc.. The device is a Class 2 Cardiovascular device with product code DSB cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K970603 · Cmc Sense-It, Inc. · Cardiovascular device
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Apr 1997
Decision
42d
Days
Class 2
Risk

K970603 is an FDA 510(k) clearance for the D SERIES ELECTRODE. Classified as Plethysmograph, Impedance (product code DSB), Class II - Special Controls.

Submitted by Cmc Sense-It, Inc. (Hopkins, US). The FDA issued a Cleared decision on April 1, 1997 after a review of 42 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2770 - 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 Cmc Sense-It, Inc. devices

FDA 510(k) Submission Details - K970603

510(k) Number K970603 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 18, 1997
Decision Date April 01, 1997
Days to Decision 42 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
83d faster than avg
Panel avg: 125d · This submission: 42d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DSB Device Classification - Class 2, Special Controls

Product Code DSB Plethysmograph, Impedance
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2770
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 - DSB Plethysmograph, Impedance

All 25
Devices cleared under the same product code (DSB) and FDA review panel - the closest regulatory comparables to K970603.
ICG MODULE
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PERCUPUMP II WITH EDA
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PROCORD MD3500 VASCULAR DIAGNOSTIC SYSTEM
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DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS
K881841 · Buckman Co., Inc. · Dec 1988