Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MERIUAARA & ERACARE WHEELCHAIRS

K-Number: K851553 · 1985-07-09

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

Device Summary

MERIUAARA & ERACARE WHEELCHAIRS 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 K851553. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIUAARA & ERACARE WHEELCHAIRS?

MERIUAARA & ERACARE WHEELCHAIRS 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 K851553.

When did MERIUAARA & ERACARE WHEELCHAIRS receive FDA 510(k) clearance?

MERIUAARA & ERACARE WHEELCHAIRS received FDA 510(k) clearance on 1985-07-09, under 510(k) number K851553.

Who is the listed applicant for MERIUAARA & ERACARE WHEELCHAIRS?

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 MERIUAARA & ERACARE WHEELCHAIRS?

The FDA product code for MERIUAARA & ERACARE WHEELCHAIRS is IOR.

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: IOR)

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.

↑