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FDA 510(k)

DEFIBRILLATOR ANALYZER, DELTA 1000

K-Number: K961595 · 1996-10-29

ApplicantNetech Corp.
Decision Date1996-10-29
Product CodeDRL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DEFIBRILLATOR ANALYZER, DELTA 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Netech Corp.. It received FDA 510(k) clearance on 1996-10-29 under 510(k) number K961595. The device is classified under product code DRL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEFIBRILLATOR ANALYZER, DELTA 1000?

DEFIBRILLATOR ANALYZER, DELTA 1000 is a medical device that received FDA 510(k) clearance on 1996-10-29. The listed applicant is Netech Corp.. The 510(k) number is K961595.

When did DEFIBRILLATOR ANALYZER, DELTA 1000 receive FDA 510(k) clearance?

DEFIBRILLATOR ANALYZER, DELTA 1000 received FDA 510(k) clearance on 1996-10-29, under 510(k) number K961595.

Who is the listed applicant for DEFIBRILLATOR ANALYZER, DELTA 1000?

The FDA 510(k) record lists Netech Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEFIBRILLATOR ANALYZER, DELTA 1000?

The FDA product code for DEFIBRILLATOR ANALYZER, DELTA 1000 is DRL.

Related Clinical Trials

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Related Devices (Code: DRL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K190437Delta 3300Netech CorporationK182905UniPulseSeaward GroupK110192DEFIBRILLATOR ANALYZER - DA-2006PBc Group International, Inc.K083347IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADSFluke BiomedicalK072114IMPULSE 6000D/7000DPFluke BiomedicalK062099PHASE 3, MODEL DT-1Datrend Systems, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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