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FDA 510(k)

EK COMBI MSG-1

K-Number: K830410 · 1983-04-27

ApplicantJedmed Instrument Co.
Decision Date1983-04-27
Product CodeDSP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EK COMBI MSG-1 is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1983-04-27 under 510(k) number K830410. The device is classified under product code DSP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EK COMBI MSG-1?

EK COMBI MSG-1 is a medical device that received FDA 510(k) clearance on 1983-04-27. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K830410.

When did EK COMBI MSG-1 receive FDA 510(k) clearance?

EK COMBI MSG-1 received FDA 510(k) clearance on 1983-04-27, under 510(k) number K830410.

Who is the listed applicant for EK COMBI MSG-1?

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

What is the FDA product code for EK COMBI MSG-1?

The FDA product code for EK COMBI MSG-1 is DSP.

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Other records listing Jedmed Instrument Co. 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.

K021750LID CHAIN EYELID WEIGHTSK954184JED-LIGHT FIBEROPTIC LIGHT SOURCEK944032VIDEO SCOPE SYSTEM (LARYNGOSCOPE)K950925JEDMED LARYNGEAL SCOPEK953457JEDMED SPECTRUM ENT CABINETK950785HORTMANN AIRMATIC AIR CALORIC STIMULATOR

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Related Devices (Code: DSP)

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.

K250542AC3™ Range™ Intra-Aortic Balloon PumpArrow International, LLCK232343AC3™ Series IABPArrow International, LLCK201112AC3 IABP, AC3 Optimus IABP, AutoCAT2 Wave IABP, AutoCAT2 IABPArrow International, Inc.K200634Arrow FiberOptix Intra-Aortic Balloon Catheter KitArrow International, Inc.K192238AC3 Series Intra-Aortic Balloon Pump (IABP)Arrow International, TeleflexK190101UltraFlex IABArrow International, 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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