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

CARDIMAX FX-1164

K Number: K853979 · Decision Feb 6, 1986
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
21
Review Days
133

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Basic Information

Device Name
CARDIMAX FX-1164
K Number
K853979
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Brentwood Instruments, Inc.
Date Received
September 26, 1985
Decision Date
February 6, 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

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Other Clearances by Brentwood Instruments, Inc.

K Number Device Name
K896924 SPIROSCAN 4000
K882366 RHYTHMSCAN HR HOLTER RECORDER
K871572 RHYTHMSCAN
K860024 FUKUDA DENSHI CARDIMAX FCP-211
K854505 CARDIMAX FX-406U
K851135 SPIRO SCAN
K851124 T-1000 ECG TRANSMITTER
K851123 R-1000 ECG RECEIVER
K842976 BRENTWOOD EZ SCAN 200 AMBULATORY ECG
K844470 FUKUDA DENSHI MODEL FCP-220
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