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FDA 510(k)

JUERGENS SELF RELIANT WHEELCHAIR

K-Number: K860072 · 1986-01-13

Decision Date1986-01-13
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JUERGENS SELF RELIANT WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is E.H. Juergens, Inc.. It received FDA 510(k) clearance on 1986-01-13 under 510(k) number K860072. 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 JUERGENS SELF RELIANT WHEELCHAIR?

JUERGENS SELF RELIANT WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1986-01-13. The listed applicant is E.H. Juergens, Inc.. The 510(k) number is K860072.

When did JUERGENS SELF RELIANT WHEELCHAIR receive FDA 510(k) clearance?

JUERGENS SELF RELIANT WHEELCHAIR received FDA 510(k) clearance on 1986-01-13, under 510(k) number K860072.

Who is the listed applicant for JUERGENS SELF RELIANT WHEELCHAIR?

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

What is the FDA product code for JUERGENS SELF RELIANT WHEELCHAIR?

The FDA product code for JUERGENS SELF RELIANT WHEELCHAIR 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.

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

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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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