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FDA 510(k)

BEDSIDE CADDY

K-Number: K925234 · 1993-11-19

ApplicantResearched, Novel Medical Devices (Rn/Md)
Decision Date1993-11-19
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BEDSIDE CADDY is the device name listed in this FDA 510(k) record. The listed applicant is Researched, Novel Medical Devices (Rn/Md). It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K925234. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEDSIDE CADDY?

BEDSIDE CADDY is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is Researched, Novel Medical Devices (Rn/Md). The 510(k) number is K925234.

When did BEDSIDE CADDY receive FDA 510(k) clearance?

BEDSIDE CADDY received FDA 510(k) clearance on 1993-11-19, under 510(k) number K925234.

Who is the listed applicant for BEDSIDE CADDY?

The FDA 510(k) record lists Researched, Novel Medical Devices (Rn/Md) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEDSIDE CADDY?

The FDA product code for BEDSIDE CADDY is FMI.

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Other records listing Researched, Novel Medical Devices (Rn/Md) as applicant

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Related Devices (Code: FMI)

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.

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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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