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)

OCTOSTOP(R) CHAIR (NEW MODEL

K-Number: K935444 · 1994-09-02

Decision Date1994-09-02
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OCTOSTOP(R) CHAIR (NEW MODEL is the device name listed in this FDA 510(k) record. The listed applicant is Octostop, Inc.. It received FDA 510(k) clearance on 1994-09-02 under 510(k) number K935444. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCTOSTOP(R) CHAIR (NEW MODEL?

OCTOSTOP(R) CHAIR (NEW MODEL is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Octostop, Inc.. The 510(k) number is K935444.

When did OCTOSTOP(R) CHAIR (NEW MODEL receive FDA 510(k) clearance?

OCTOSTOP(R) CHAIR (NEW MODEL received FDA 510(k) clearance on 1994-09-02, under 510(k) number K935444.

Who is the listed applicant for OCTOSTOP(R) CHAIR (NEW MODEL?

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

What is the FDA product code for OCTOSTOP(R) CHAIR (NEW MODEL?

The FDA product code for OCTOSTOP(R) CHAIR (NEW MODEL is IXR.

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 Octostop, 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 13 devices →

Related Devices (Code: IXR)

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.

↑