DALE ENDOTRACHEAL TUBE HOLDER
K-Number: K832946 · 1983-10-14
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Device Summary
Frequently Asked Questions
What is the DALE ENDOTRACHEAL TUBE HOLDER?
DALE ENDOTRACHEAL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Dale Medical Products, Inc.. The 510(k) number is K832946.
When did DALE ENDOTRACHEAL TUBE HOLDER receive FDA 510(k) clearance?
DALE ENDOTRACHEAL TUBE HOLDER received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832946.
Who is the listed applicant for DALE ENDOTRACHEAL TUBE HOLDER?
The FDA 510(k) record lists Dale Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DALE ENDOTRACHEAL TUBE HOLDER?
The FDA product code for DALE 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 Dale Medical 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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