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FDA 510(k)

SHERIDAN/ESOPHAGEAL STETHOSCOPE

K-Number: K830218 · 1983-03-09

Decision Date1983-03-09
Product CodeBZW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SHERIDAN/ESOPHAGEAL STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Sheridan Catheter Corp.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K830218. The device is classified under product code BZW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 39 devices →

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

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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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