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FDA 510(k)

EGERTON TURNING & TILTING NET SUSPEN BED

K-Number: K832845 · 1983-11-28

Decision Date1983-11-28
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EGERTON TURNING & TILTING NET SUSPEN BED is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Concepts, Inc.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K832845. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 48 devices →

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

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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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