TUBMATE
K-Number: K811301 · 1981-05-27
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Device Summary
Frequently Asked Questions
What is the TUBMATE?
TUBMATE is a medical device that received FDA 510(k) clearance on 1981-05-27. The listed applicant is American Stair-Glide Corp.. The 510(k) number is K811301.
When did TUBMATE receive FDA 510(k) clearance?
TUBMATE received FDA 510(k) clearance on 1981-05-27, under 510(k) number K811301.
Who is the listed applicant for TUBMATE?
The FDA 510(k) record lists American Stair-Glide Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBMATE?
The FDA product code for TUBMATE is ILS.
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 American Stair-Glide Corp. 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: ILS)
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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