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

CIRCAMED HOLTER VERSION 4

K Number: K894956 · Decision Feb 5, 1990
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
13
Review Days
185

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
CIRCAMED HOLTER VERSION 4
K Number
K894956
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Circadian, Inc.
Date Received
August 4, 1989
Decision Date
February 5, 1990
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 Circadian, Inc.

K Number Device Name
K921878 SCANMATE III
K874641 CIRCADIAN STRESS TEST II
K874155 CIRCAMED MONITOR REMOTE START CONDUCTANCE METER
K871251 CIRCAMED FULL DISCLOSURE SYSTEM
K860973 CIRCADIAN STRESS TEST SYSTEM
K851517 CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITO
K851643 REMOTE CONTROL MODULE
K840741 PULMONARY FUNCTION TESTING STS
K833619 CONDUCTANCE METER
K830830 CIRCA MED TWO-CHANNEL
Search all 13 clearances from Circadian, Inc. →