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FDA 510(k)

CADISCOPE ELECTRONIC STETHOSCOPE

K-Number: K990809 · 1999-06-09

ApplicantCaditec AG
Decision Date1999-06-09
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CADISCOPE ELECTRONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Caditec AG. It received FDA 510(k) clearance on 1999-06-09 under 510(k) number K990809. 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 CADISCOPE ELECTRONIC STETHOSCOPE?

CADISCOPE ELECTRONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1999-06-09. The listed applicant is Caditec AG. The 510(k) number is K990809.

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

CADISCOPE ELECTRONIC STETHOSCOPE received FDA 510(k) clearance on 1999-06-09, under 510(k) number K990809.

Who is the listed applicant for CADISCOPE ELECTRONIC STETHOSCOPE?

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

What is the FDA product code for CADISCOPE ELECTRONIC STETHOSCOPE?

The FDA product code for CADISCOPE ELECTRONIC STETHOSCOPE is DQD.

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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.

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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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