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FDA 510(k)

MIL CM-II COAGULATION MACHINE

K-Number: K913320 · 1992-06-16

ApplicantMedical Innovations Corp.
Decision Date1992-06-16
Product CodeGKN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MIL CM-II COAGULATION MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Innovations Corp.. It received FDA 510(k) clearance on 1992-06-16 under 510(k) number K913320. The device is classified under product code GKN. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIL CM-II COAGULATION MACHINE?

MIL CM-II COAGULATION MACHINE is a medical device that received FDA 510(k) clearance on 1992-06-16. The listed applicant is Medical Innovations Corp.. The 510(k) number is K913320.

When did MIL CM-II COAGULATION MACHINE receive FDA 510(k) clearance?

MIL CM-II COAGULATION MACHINE received FDA 510(k) clearance on 1992-06-16, under 510(k) number K913320.

Who is the listed applicant for MIL CM-II COAGULATION MACHINE?

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

What is the FDA product code for MIL CM-II COAGULATION MACHINE?

The FDA product code for MIL CM-II COAGULATION MACHINE is GKN.

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Other records listing Medical Innovations 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.

K945612MIC NASOGASTRIC-GASTROJEJUNAL FEEDING TUBEK940548MIC PERCUTANEOUS ENDOSCOPIC JEJUNAL FEEDING TUBEK943685MIC DISPOSABLE SNAREK926581MIC TRANSGASTRIC JEJUNAL TUBEK921370MIC GASTRO-ENTEROSTOMY TUBE MODIFICATIONK921652MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT

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Related Devices (Code: GKN)

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.

K953870ACTTRAC ELECTRONIC CONTROL DEVICE FOR THE ACT & ACT II COAGULATION INSTRUMENTSMedtronic VascularK940426MEDTRONIC HEMOTEC ACT II AUTOMATED COAGULATION TIMERMedtronic Hemotec, 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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