VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE
K-Number: K885347 · 1989-01-30
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Device Summary
Frequently Asked Questions
What is the VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE?
VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1989-01-30. The listed applicant is Vitacomm, Inc.. The 510(k) number is K885347.
When did VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE receive FDA 510(k) clearance?
VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE received FDA 510(k) clearance on 1989-01-30, under 510(k) number K885347.
Who is the listed applicant for VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE?
The FDA 510(k) record lists Vitacomm, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE?
The FDA product code for VITACOMM MODEL #140/141 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 Vitacomm, 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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