Cleared Special

K993799 - CG-7000DX ECG RECORDER/TRANSMITTER

K993799 is an FDA 510(k) clearance for CG-7000DX ECG RECORDER/TRANSMITTER, manufactured by Card Guard Scientific Survival , Ltd.. The device is a Class 2 Cardiovascular device with product code DXH cleared through the Special 510(k) pathway after a 31-day FDA review.

K993799 · Card Guard Scientific Survival , Ltd. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1999
Decision
31d
Days
Class 2
Risk

K993799 is an FDA 510(k) clearance for the CG-7000DX ECG RECORDER/TRANSMITTER. Classified as Transmitters And Receivers, Electrocardiograph, Telephone (product code DXH), Class II - Special Controls.

Submitted by Card Guard Scientific Survival , Ltd. (Rehovot, IL). The FDA issued a Cleared decision on December 10, 1999 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2920 - the FDA cardiovascular device oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Card Guard Scientific Survival , Ltd. devices

FDA 510(k) Submission Details - K993799

510(k) Number K993799 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 09, 1999
Decision Date December 10, 1999
Days to Decision 31 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 125d · This submission: 31d
Pathway characteristics
Modification to existing cleared device.

DXH Device Classification - Class 2, Special Controls

Product Code DXH Transmitters And Receivers, Electrocardiograph, Telephone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2920
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 - DXH Transmitters And Receivers, Electrocardiograph, Telephone

All 115
Devices cleared under the same product code (DXH) and FDA review panel - the closest regulatory comparables to K993799.
PERSONAL ECG TRANSMITTER, MODEL CG-6550
K003220 · Card Guard Scientific Survival , Ltd. · Nov 2000
CARD GUARD PERSONAL ELECTROCARDIOGRAM TRANSMITTER, MODEL CG-6206/6306
K000225 · Card Guard Scientific Survival , Ltd. · Feb 2000
CG-2100 ECG TRANSMITTER
K994009 · Card Guard Scientific Survival , Ltd. · Dec 1999
ECG MINIMONITOR, MODEL CG-5000
K992696 · Card Guard Scientific Survival , Ltd. · Oct 1999
CARD GUARD, MODEL CG-6550
K990478 · Card Guard Scientific Survival , Ltd. · Aug 1999
TELEMEDICINE 2000
K992164 · Card Guard Scientific Survival , Ltd. · Aug 1999