MASCOT STETHOSCOPE PROBE
K-Number: K874726 · 1988-03-31
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Device Summary
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.
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.
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