NESBIT EVANS NURSING HOME BED
K-Number: K864203 · 1986-11-07
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Device Summary
Frequently Asked Questions
What is the NESBIT EVANS NURSING HOME BED?
NESBIT EVANS NURSING HOME BED is a medical device that received FDA 510(k) clearance on 1986-11-07. The listed applicant is J. Nesbit Evans & Co.. The 510(k) number is K864203.
When did NESBIT EVANS NURSING HOME BED receive FDA 510(k) clearance?
NESBIT EVANS NURSING HOME BED received FDA 510(k) clearance on 1986-11-07, under 510(k) number K864203.
Who is the listed applicant for NESBIT EVANS NURSING HOME BED?
The FDA 510(k) record lists J. Nesbit Evans & Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NESBIT EVANS NURSING HOME BED?
The FDA product code for NESBIT EVANS NURSING HOME BED is FNJ.
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.
Related Devices (Code: FNJ)
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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