DEFIBRILLATOR ANALYZER, DELTA 1000— 510(k) K961595

Name: FDA 510(k) clearance K961595
Creator: U.S. Food and Drug Administration
Published: 1996-10-29

Substantially Equivalent

Netech Corp.

FDA 510(k) clearance K961595 for DEFIBRILLATOR ANALYZER, DELTA 1000, Substantially Equivalent on 1996-10-29. Applicant: Netech Corp.. Device class: 2.

Clearance details

Applicant: Netech Corp.
Product code: Code DRL
Device class: Class 2
Regulation: 21 CFR 870.5325
Advisory panel: Cardiovascular
Date received: 1996-04-24
Decision date: 1996-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sound Beach, NY, US

Download summary PDF View on FDA.gov ↗

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