ASCENDA
K-Number: K941642 · 1994-06-13
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Device Summary
Frequently Asked Questions
What is the ASCENDA?
ASCENDA is a medical device that received FDA 510(k) clearance on 1994-06-13. The listed applicant is American Stair-Glide Corp.. The 510(k) number is K941642.
When did ASCENDA receive FDA 510(k) clearance?
ASCENDA received FDA 510(k) clearance on 1994-06-13, under 510(k) number K941642.
Who is the listed applicant for ASCENDA?
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 ASCENDA?
The FDA product code for ASCENDA is ING.
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: ING)
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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