EGERTON TURNING & TILTING NET SUSPEN BED
K-Number: K832845 · 1983-11-28
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Device Summary
Frequently Asked Questions
What is the EGERTON TURNING & TILTING NET SUSPEN BED?
EGERTON TURNING & TILTING NET SUSPEN BED is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K832845.
When did EGERTON TURNING & TILTING NET SUSPEN BED receive FDA 510(k) clearance?
EGERTON TURNING & TILTING NET SUSPEN BED received FDA 510(k) clearance on 1983-11-28, under 510(k) number K832845.
Who is the listed applicant for EGERTON TURNING & TILTING NET SUSPEN BED?
The FDA 510(k) record lists Kinetic Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EGERTON TURNING & TILTING NET SUSPEN BED?
The FDA product code for EGERTON TURNING & TILTING NET SUSPEN 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.
Other records listing Kinetic Concepts, 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: 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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