DEFIBRILLATOR ANALYZER, DELTA 1000— 510(k) K961595

Substantially Equivalent

Netech Corp.

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

Clearance details

Applicant: Netech Corp.
Product code: Code DRL
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 ↗

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