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FDA 510(k)

ADC 656 ELECTRONIC STETHOSCOPE

K-Number: K012304 · 2001-11-01

ApplicantAmerican Diagnostic Corp.
Decision Date2001-11-01
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADC 656 ELECTRONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is American Diagnostic Corp.. It received FDA 510(k) clearance on 2001-11-01 under 510(k) number K012304. 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 ADC 656 ELECTRONIC STETHOSCOPE?

ADC 656 ELECTRONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2001-11-01. The listed applicant is American Diagnostic Corp.. The 510(k) number is K012304.

When did ADC 656 ELECTRONIC STETHOSCOPE receive FDA 510(k) clearance?

ADC 656 ELECTRONIC STETHOSCOPE received FDA 510(k) clearance on 2001-11-01, under 510(k) number K012304.

Who is the listed applicant for ADC 656 ELECTRONIC STETHOSCOPE?

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

What is the FDA product code for ADC 656 ELECTRONIC STETHOSCOPE?

The FDA product code for ADC 656 ELECTRONIC STETHOSCOPE is DQD.

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Other records listing American Diagnostic Corp. 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.

K162589Adscope 658 Electronic StethoscopeK093495OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITSK060321ADSCOPE 657BK ELECTRONIC STETHOSCOPE, MODEL 657BKK962655ANEROID AND MERCURIAL SPHYGMOMANOMETERSK940686ELECTRONIC THERMOMETERSK935944PROSCOPES AND ADSCOPES

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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

View on FDA Database →

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

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