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FDA 510(k)

MX2 ELECTRONIC STETHOSCOPE

K-Number: K842705 · 1985-01-23

ApplicantMedmax, Inc.
Decision Date1985-01-23
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MX2 ELECTRONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Medmax, Inc.. It received FDA 510(k) clearance on 1985-01-23 under 510(k) number K842705. 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 MX2 ELECTRONIC STETHOSCOPE?

MX2 ELECTRONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1985-01-23. The listed applicant is Medmax, Inc.. The 510(k) number is K842705.

When did MX2 ELECTRONIC STETHOSCOPE receive FDA 510(k) clearance?

MX2 ELECTRONIC STETHOSCOPE received FDA 510(k) clearance on 1985-01-23, under 510(k) number K842705.

Who is the listed applicant for MX2 ELECTRONIC STETHOSCOPE?

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

What is the FDA product code for MX2 ELECTRONIC STETHOSCOPE?

The FDA product code for MX2 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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