DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE
K-Number: K925789 · 1993-07-13
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Device Summary
Frequently Asked Questions
What is the DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE?
DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K925789.
When did DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE receive FDA 510(k) clearance?
DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE received FDA 510(k) clearance on 1993-07-13, under 510(k) number K925789.
Who is the listed applicant for DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE?
The FDA 510(k) record lists Deroyal Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE?
The FDA product code for DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE is BZT.
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 Deroyal Industries, 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: BZT)
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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