Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MASCOT STETHOSCOPE PROBE

K-Number: K874726 · 1988-03-31

Decision Date1988-03-31
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MASCOT STETHOSCOPE PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Imex Medical Systems, Inc.. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K874726. 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 MASCOT STETHOSCOPE PROBE?

MASCOT STETHOSCOPE PROBE is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Imex Medical Systems, Inc.. The 510(k) number is K874726.

When did MASCOT STETHOSCOPE PROBE receive FDA 510(k) clearance?

MASCOT STETHOSCOPE PROBE received FDA 510(k) clearance on 1988-03-31, under 510(k) number K874726.

Who is the listed applicant for MASCOT STETHOSCOPE PROBE?

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

What is the FDA product code for MASCOT STETHOSCOPE PROBE?

The FDA product code for MASCOT STETHOSCOPE PROBE is DQD.

Related Clinical Trials

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.

Other records listing Imex Medical Systems, Inc. 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.

View all 19 devices →

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.

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.

↑