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FDA 510(k)

MERIVAARA GERIATRIC CHAIR

K-Number: K851550 · 1985-07-09

Decision Date1985-07-09
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MERIVAARA GERIATRIC CHAIR 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 1985-07-09 under 510(k) number K851550. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIVAARA GERIATRIC CHAIR?

MERIVAARA GERIATRIC CHAIR is a medical device that received FDA 510(k) clearance on 1985-07-09. The listed applicant is Daun International, Inc.. The 510(k) number is K851550.

When did MERIVAARA GERIATRIC CHAIR receive FDA 510(k) clearance?

MERIVAARA GERIATRIC CHAIR received FDA 510(k) clearance on 1985-07-09, under 510(k) number K851550.

Who is the listed applicant for MERIVAARA GERIATRIC CHAIR?

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 GERIATRIC CHAIR?

The FDA product code for MERIVAARA GERIATRIC CHAIR is INM.

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: INM)

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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