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FDA 510(k)

E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120

K-Number: K961301 · 1996-06-11

ApplicantDelphi Consulting Group
Decision Date1996-06-11
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120 is the device name listed in this FDA 510(k) record. The listed applicant is Delphi Consulting Group. It received FDA 510(k) clearance on 1996-06-11 under 510(k) number K961301. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120?

E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120 is a medical device that received FDA 510(k) clearance on 1996-06-11. The listed applicant is Delphi Consulting Group. The 510(k) number is K961301.

When did E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120 receive FDA 510(k) clearance?

E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120 received FDA 510(k) clearance on 1996-06-11, under 510(k) number K961301.

Who is the listed applicant for E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120?

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

What is the FDA product code for E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120?

The FDA product code for E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120 is DQD.

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Other records listing Delphi Consulting Group as applicant

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.

K983680TRINITY II SINGLE CHAMBER DVT PUMPK963957TRINITY DVT SYSTEMK970014TRINITY SLEEVES, HUNTLEIGH PUMP COMPATIBLE(T.B.D.)K961937SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEMK954489TRINITY SLEEVE(S)

Related Devices (Code: DQD)

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.

K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730)Shanghai Hulu Devices Co., Ltd.K261694CORE 300 Digital StethoscopeEko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089Tyto Stethoscope (G3)Tyto Care , Ltd.K252076Kneevoice Cartilage Evaluation System (750-3600-001)Kneevoice, Inc.K252284eMurmur Heart AICsd Labs

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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