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FDA 510(k)

JEOL MODEL #JTG-500M

K-Number: K823041 · 1982-11-24

ApplicantJeol
Decision Date1982-11-24
Product CodeIYM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JEOL MODEL #JTG-500M is the device name listed in this FDA 510(k) record. The listed applicant is Jeol. It received FDA 510(k) clearance on 1982-11-24 under 510(k) number K823041. The device is classified under product code IYM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JEOL MODEL #JTG-500M?

JEOL MODEL #JTG-500M is a medical device that received FDA 510(k) clearance on 1982-11-24. The listed applicant is Jeol. The 510(k) number is K823041.

When did JEOL MODEL #JTG-500M receive FDA 510(k) clearance?

JEOL MODEL #JTG-500M received FDA 510(k) clearance on 1982-11-24, under 510(k) number K823041.

Who is the listed applicant for JEOL MODEL #JTG-500M?

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

What is the FDA product code for JEOL MODEL #JTG-500M?

The FDA product code for JEOL MODEL #JTG-500M is IYM.

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Related Devices (Code: IYM)

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.

K863736FMS MODEL 110Flir Medical SystemsK852950VISITHERMC.D. Regelin & Associates, Inc.K812799DCATSDorex, Inc.K812701ORTHO-THERM INFRARED SENSOROrthion Corp.K801553THERMOCOMPHospital Financial Corp.K800491GRAPHIC STRESS TELETHERMOMETRYGst Laboratories of Ca, Inc.

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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