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)

ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS

K-Number: K874295 · 1987-11-24

Decision Date1987-11-24
Product CodeBZT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS 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 1987-11-24 under 510(k) number K874295. The device is classified under product code BZT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS?

ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS is a medical device that received FDA 510(k) clearance on 1987-11-24. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K874295.

When did ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS receive FDA 510(k) clearance?

ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS received FDA 510(k) clearance on 1987-11-24, under 510(k) number K874295.

Who is the listed applicant for ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS?

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 ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS?

The FDA product code for ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS 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 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: 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.

↑