FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MODEL 456 ELECTROCARDIORECORDER RECORDER

K Number: K863652 · Decision Dec 10, 1986
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
54
Review Days
83

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MODEL 456 ELECTROCARDIORECORDER RECORDER
K Number
K863652
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Del Mar Avionics
Date Received
September 18, 1986
Decision Date
December 10, 1986
Product Code
DPS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPS Electrocardiograph

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DPS), ordered by most recent decision date.

View all

Other Clearances by Del Mar Avionics

K Number Device Name
K990027 OMNICORDER, MODEL 464
K971696 SENTINEL RECORDER, MODELS 471/472
K963174 HOLTER DIGICORDER WITH PACER OPTION (MODEL 483)
K950020 HOLTER PACERCORDER(R)
K942653 HOLTER SSR DIGICORDER(TM)
K922221 SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM
K896862 MODEL 263 SPECTRASCAN(TM) HOLTER ANALYSIS SYSTEM
K895793 MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION
K894543 MODEL 493 SSR-3 THREE CHANNEL SOLID-STATE RECORDER
K891148 MODEL 152 DELTA HOLTER ECG ANALYSIS SYSTEM
Search all 54 clearances from Del Mar Avionics →