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FDA 510(k)

ASCENDA

K-Number: K941642 · 1994-06-13

Decision Date1994-06-13
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ASCENDA is the device name listed in this FDA 510(k) record. The listed applicant is American Stair-Glide Corp.. It received FDA 510(k) clearance on 1994-06-13 under 510(k) number K941642. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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