CUSHION, WHELCHAR AND FLOTATION
K-Number: K915629 · 1992-01-09
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Device Summary
Frequently Asked Questions
What is the CUSHION, WHELCHAR AND FLOTATION?
CUSHION, WHELCHAR AND FLOTATION is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Invacare Corp.. The 510(k) number is K915629.
When did CUSHION, WHELCHAR AND FLOTATION receive FDA 510(k) clearance?
CUSHION, WHELCHAR AND FLOTATION received FDA 510(k) clearance on 1992-01-09, under 510(k) number K915629.
Who is the listed applicant for CUSHION, WHELCHAR AND FLOTATION?
The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUSHION, WHELCHAR AND FLOTATION?
The FDA product code for CUSHION, WHELCHAR AND FLOTATION is KNN.
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 Invacare 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: KNN)
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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