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FDA 510(k)

MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES

K-Number: K851551 · 1985-05-08

Decision Date1985-05-08
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Daun International, Inc.. It received FDA 510(k) clearance on 1985-05-08 under 510(k) number K851551. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES?

MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1985-05-08. The listed applicant is Daun International, Inc.. The 510(k) number is K851551.

When did MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES receive FDA 510(k) clearance?

MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES received FDA 510(k) clearance on 1985-05-08, under 510(k) number K851551.

Who is the listed applicant for MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES?

The FDA 510(k) record lists Daun International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES?

The FDA product code for MERIVAARA ELECTRIC HOSPITAL BED & ACCESSORIES is FNL.

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 Daun International, 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 7 devices →

Related Devices (Code: FNL)

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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