AMPLIFIER MODEL N5A-ECG— 510(k) K771684

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K771684 for AMPLIFIER MODEL N5A-ECG, Substantially Equivalent on 1977-09-14. Applicant: Honeywell, Inc.. Device class: 1.

Clearance details

Applicant: Honeywell, Inc.
Product code: Code DRJ
Device class: Class 1
Regulation: 21 CFR 870.2600
Advisory panel: Cardiovascular
Date received: 1977-09-06
Decision date: 1977-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DRJ

K832828 — CENTURION CARDIAC DETECTOR1984-05-09
K822590 — PRESSURE ISOLATION AMPLIFIER #9813 5171982-10-04
K771685 — AMPLIFIER MODEL N5A-HIS1977-09-14

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Data sourced from openFDA. This site is unofficial and independent of the FDA.