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FDA 510(k)

COAGULATOR (8 CHANNEL)

K-Number: K862047 · 1986-09-29

ApplicantMed USA
Decision Date1986-09-29
Product CodeKQG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

COAGULATOR (8 CHANNEL) is the device name listed in this FDA 510(k) record. The listed applicant is Med USA. It received FDA 510(k) clearance on 1986-09-29 under 510(k) number K862047. The device is classified under product code KQG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAGULATOR (8 CHANNEL)?

COAGULATOR (8 CHANNEL) is a medical device that received FDA 510(k) clearance on 1986-09-29. The listed applicant is Med USA. The 510(k) number is K862047.

When did COAGULATOR (8 CHANNEL) receive FDA 510(k) clearance?

COAGULATOR (8 CHANNEL) received FDA 510(k) clearance on 1986-09-29, under 510(k) number K862047.

Who is the listed applicant for COAGULATOR (8 CHANNEL)?

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

What is the FDA product code for COAGULATOR (8 CHANNEL)?

The FDA product code for COAGULATOR (8 CHANNEL) is KQG.

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 Med USA 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.

K896766TD-28 DISPOSABLE ELECTRODEK852492COAGULATORK850711INHALATION THERAPY NEBULIZER DEVICEK841803A1 SYSTEME 8201/2

Related Devices (Code: KQG)

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.

K050821COAGCARE ANTICOAGULATION MANAGEMENT SYSTEMZycareK021976FIBRON-1, FIBRON-4, QUIKCOAG, FIBRONVital Scientific N.V.K992130PACIFIC HEMOSTASIS THROMBOSCREEN 400CPacific HemostasisK991321PACIFIC HEMOSTASIS THROMBOSCREEN 200Pacific HemostasisK983475HEMOCHRON RESPONSEInternational Technidyne Corp.K902614ELVI 828 DIGICLOT MULTISCANLogos Scientific, 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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