CONVALESCENT RECLINER
K-Number: K802803 · 1980-11-19
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Device Summary
Frequently Asked Questions
What is the CONVALESCENT RECLINER?
CONVALESCENT RECLINER is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Winfield Co., Inc.. The 510(k) number is K802803.
When did CONVALESCENT RECLINER receive FDA 510(k) clearance?
CONVALESCENT RECLINER received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802803.
Who is the listed applicant for CONVALESCENT RECLINER?
The FDA 510(k) record lists Winfield Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONVALESCENT RECLINER?
The FDA product code for CONVALESCENT RECLINER is INO.
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 Winfield Co., 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: INO)
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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