ENDOTRACHEAL TUBE HOLDER
K-Number: K802675 · 1980-11-19
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Device Summary
Frequently Asked Questions
What is the ENDOTRACHEAL TUBE HOLDER?
ENDOTRACHEAL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K802675.
When did ENDOTRACHEAL TUBE HOLDER receive FDA 510(k) clearance?
ENDOTRACHEAL TUBE HOLDER received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802675.
Who is the listed applicant for ENDOTRACHEAL TUBE HOLDER?
The FDA 510(k) record lists Respiratory Support Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOTRACHEAL TUBE HOLDER?
The FDA product code for ENDOTRACHEAL TUBE HOLDER is JAY.
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 Respiratory Support Products, 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: JAY)
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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