SHERIDAN/ESOPHAGEAL STETHOSCOPE
K-Number: K830218 · 1983-03-09
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Device Summary
Frequently Asked Questions
What is the SHERIDAN/ESOPHAGEAL STETHOSCOPE?
SHERIDAN/ESOPHAGEAL STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K830218.
When did SHERIDAN/ESOPHAGEAL STETHOSCOPE receive FDA 510(k) clearance?
SHERIDAN/ESOPHAGEAL STETHOSCOPE received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830218.
Who is the listed applicant for SHERIDAN/ESOPHAGEAL STETHOSCOPE?
The FDA 510(k) record lists Sheridan Catheter Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHERIDAN/ESOPHAGEAL STETHOSCOPE?
The FDA product code for SHERIDAN/ESOPHAGEAL STETHOSCOPE is BZW.
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 Sheridan Catheter Corp. 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: BZW)
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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