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)

RLS 9100 RHINO-LARYNGEAL STROBOSCOPE

K-Number: K921184 · 1992-05-28

ApplicantKay Elemetrics Corp.
Decision Date1992-05-28
Product CodeEQL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RLS 9100 RHINO-LARYNGEAL STROBOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Kay Elemetrics Corp.. It received FDA 510(k) clearance on 1992-05-28 under 510(k) number K921184. The device is classified under product code EQL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RLS 9100 RHINO-LARYNGEAL STROBOSCOPE?

RLS 9100 RHINO-LARYNGEAL STROBOSCOPE is a medical device that received FDA 510(k) clearance on 1992-05-28. The listed applicant is Kay Elemetrics Corp.. The 510(k) number is K921184.

When did RLS 9100 RHINO-LARYNGEAL STROBOSCOPE receive FDA 510(k) clearance?

RLS 9100 RHINO-LARYNGEAL STROBOSCOPE received FDA 510(k) clearance on 1992-05-28, under 510(k) number K921184.

Who is the listed applicant for RLS 9100 RHINO-LARYNGEAL STROBOSCOPE?

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

What is the FDA product code for RLS 9100 RHINO-LARYNGEAL STROBOSCOPE?

The FDA product code for RLS 9100 RHINO-LARYNGEAL STROBOSCOPE is EQL.

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 Kay Elemetrics Corp. 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.

K991738DIGITAL VIDEO RECORDING SYSTEMK990240ELECTROGLOTTOGRAPHK9547987100 SWALLOWING WORKSTATIONK9212859105 RIGID TELESCOPIC ENDOSCOPE

Related Devices (Code: EQL)

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.

K984521RIWO DRIVE SYSTEM 2302 WITH GENERATOR, SMALL MOTOR HANDLES, 8563.111, 8563.351Richard Wolf Medical Instruments Corp.K9212859105 RIGID TELESCOPIC ENDOSCOPEKay Elemetrics Corp.K884933ENDOSTROBOSCOPE IVJedmed Instrument Co.K842090RHINO-LARYNX STROBOSCOPE TYPE 4914Bruel & Kjaer Industri A/SK822523LARYNGOSTROBOSCOPEKelleher Corp.K801866PENTAX LARYNGO-STROBOSCOPE MODEL LS-1APentax Precision Instrument Corp.

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.

↑