MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM)
K-Number: K870255 · 1987-03-26
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Device Summary
Frequently Asked Questions
What is the MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM)?
MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM) is a medical device that received FDA 510(k) clearance on 1987-03-26. The listed applicant is Transcor, Inc.. The 510(k) number is K870255.
When did MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM) receive FDA 510(k) clearance?
MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM) received FDA 510(k) clearance on 1987-03-26, under 510(k) number K870255.
Who is the listed applicant for MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM)?
The FDA 510(k) record lists Transcor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM)?
The FDA product code for MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM) 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 Transcor, 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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