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FDA 510(k)

9105 RIGID TELESCOPIC ENDOSCOPE

K-Number: K921285 · 1992-05-28

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

Device Summary

9105 RIGID TELESCOPIC ENDOSCOPE 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 K921285. 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 9105 RIGID TELESCOPIC ENDOSCOPE?

9105 RIGID TELESCOPIC ENDOSCOPE 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 K921285.

When did 9105 RIGID TELESCOPIC ENDOSCOPE receive FDA 510(k) clearance?

9105 RIGID TELESCOPIC ENDOSCOPE received FDA 510(k) clearance on 1992-05-28, under 510(k) number K921285.

Who is the listed applicant for 9105 RIGID TELESCOPIC ENDOSCOPE?

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 9105 RIGID TELESCOPIC ENDOSCOPE?

The FDA product code for 9105 RIGID TELESCOPIC ENDOSCOPE 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.

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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 WORKSTATIONK921184RLS 9100 RHINO-LARYNGEAL STROBOSCOPE

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.K921184RLS 9100 RHINO-LARYNGEAL STROBOSCOPEKay 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.

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