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)

FISK HEADREST

K-Number: K924700 · 1993-01-15

ApplicantRhino Mfg.
Decision Date1993-01-15
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FISK HEADREST is the device name listed in this FDA 510(k) record. The listed applicant is Rhino Mfg.. It received FDA 510(k) clearance on 1993-01-15 under 510(k) number K924700. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISK HEADREST?

FISK HEADREST is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Rhino Mfg.. The 510(k) number is K924700.

When did FISK HEADREST receive FDA 510(k) clearance?

FISK HEADREST received FDA 510(k) clearance on 1993-01-15, under 510(k) number K924700.

Who is the listed applicant for FISK HEADREST?

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

What is the FDA product code for FISK HEADREST?

The FDA product code for FISK HEADREST is FQO.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Rhino Mfg. 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.

K922371SPINAL POSITIONING FRAME

Related Devices (Code: FQO)

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.

K240598Maestro System (REF100)Moon SurgicalK221410Maestro PlatformMoon SurgicalK090136STERIS CMAX XLT SURGICAL TABLESTERIS CorporationK972810OPT80 THE TRANSPORTABLE (OPT80)O.P.T. USA, Inc.K971988ALLEN, ULTRA AND SMART SOCKETSAllen Medical Systems, Inc.K971307AMSCO SURGICAL TABLESTERIS Corporation

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.

↑