SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR
K-Number: K862131 · 1986-07-14
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Device Summary
Frequently Asked Questions
What is the SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR?
SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR is a medical device that received FDA 510(k) clearance on 1986-07-14. The listed applicant is K & S Medicorp. The 510(k) number is K862131.
When did SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR receive FDA 510(k) clearance?
SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR received FDA 510(k) clearance on 1986-07-14, under 510(k) number K862131.
Who is the listed applicant for SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR?
The FDA 510(k) record lists K & S Medicorp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR?
The FDA product code for SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR 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 K & S Medicorp 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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