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FDA 510(k)

FMS MODEL 110

K-Number: K863736 · 1986-12-29

ApplicantFlir Medical Systems
Decision Date1986-12-29
Product CodeIYM
Advisory CommitteeOB
DecisionSubstantially Equivalent for Some Indications

Device Summary

FMS MODEL 110 is the device name listed in this FDA 510(k) record. The listed applicant is Flir Medical Systems. It received FDA 510(k) clearance on 1986-12-29 under 510(k) number K863736. The device is classified under product code IYM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the FMS MODEL 110?

FMS MODEL 110 is a medical device that received FDA 510(k) clearance on 1986-12-29. The listed applicant is Flir Medical Systems. The 510(k) number is K863736.

When did FMS MODEL 110 receive FDA 510(k) clearance?

FMS MODEL 110 received FDA 510(k) clearance on 1986-12-29, under 510(k) number K863736.

Who is the listed applicant for FMS MODEL 110?

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

What is the FDA product code for FMS MODEL 110?

The FDA product code for FMS MODEL 110 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.

K852950VISITHERMC.D. Regelin & Associates, Inc.K823041JEOL MODEL #JTG-500MJeolK812799DCATSDorex, 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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