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FDA 510(k)

MERIVAARA GERIATRIC CHAIR MODEL 455

K-Number: K862957 · 1986-08-21

Decision Date1986-08-21
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MERIVAARA GERIATRIC CHAIR MODEL 455 is the device name listed in this FDA 510(k) record. The listed applicant is Global Medical Prods, Inc.. It received FDA 510(k) clearance on 1986-08-21 under 510(k) number K862957. The device is classified under product code INN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIVAARA GERIATRIC CHAIR MODEL 455?

MERIVAARA GERIATRIC CHAIR MODEL 455 is a medical device that received FDA 510(k) clearance on 1986-08-21. The listed applicant is Global Medical Prods, Inc.. The 510(k) number is K862957.

When did MERIVAARA GERIATRIC CHAIR MODEL 455 receive FDA 510(k) clearance?

MERIVAARA GERIATRIC CHAIR MODEL 455 received FDA 510(k) clearance on 1986-08-21, under 510(k) number K862957.

Who is the listed applicant for MERIVAARA GERIATRIC CHAIR MODEL 455?

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

What is the FDA product code for MERIVAARA GERIATRIC CHAIR MODEL 455?

The FDA product code for MERIVAARA GERIATRIC CHAIR MODEL 455 is INN.

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 Global Medical Prods, 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 9 devices →

Related Devices (Code: INN)

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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