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FDA 510(k)

E65 35 PRONE STANDER

K-Number: K892700 · 1989-05-09

Decision Date1989-05-09
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

E65 35 PRONE STANDER is the device name listed in this FDA 510(k) record. The listed applicant is Rifton Equipment For the Handicapped. It received FDA 510(k) clearance on 1989-05-09 under 510(k) number K892700. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E65 35 PRONE STANDER?

E65 35 PRONE STANDER is a medical device that received FDA 510(k) clearance on 1989-05-09. The listed applicant is Rifton Equipment For the Handicapped. The 510(k) number is K892700.

When did E65 35 PRONE STANDER receive FDA 510(k) clearance?

E65 35 PRONE STANDER received FDA 510(k) clearance on 1989-05-09, under 510(k) number K892700.

Who is the listed applicant for E65 35 PRONE STANDER?

The FDA 510(k) record lists Rifton Equipment For the Handicapped as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E65 35 PRONE STANDER?

The FDA product code for E65 35 PRONE STANDER is INW.

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 Rifton Equipment For the Handicapped 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: INW)

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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