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FDA 510(k)

A-GENT CK-MB

K-Number: K782015 · 1979-02-01

ApplicantAbbott Laboratories
Decision Date1979-02-01
Product CodeJHW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

A-GENT CK-MB is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-02-01 under 510(k) number K782015. The device is classified under product code JHW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-GENT CK-MB?

A-GENT CK-MB is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Abbott Laboratories. The 510(k) number is K782015.

When did A-GENT CK-MB receive FDA 510(k) clearance?

A-GENT CK-MB received FDA 510(k) clearance on 1979-02-01, under 510(k) number K782015.

Who is the listed applicant for A-GENT CK-MB?

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

What is the FDA product code for A-GENT CK-MB?

The FDA product code for A-GENT CK-MB is JHW.

Other records listing Abbott Laboratories as applicant

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Related Devices (Code: JHW)

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.

K162526Creatine Kinase-MBRoche DiagnosticsK122083ELITECH CLINICAL SYSTEMS CK NAC SLElitechgroupK023744WIENER LAB. CK-MB DS UV UNITEST, MODEL 28 X 2.5 ML CAT. NR. 1271354Wiener Laboratories SaicK003158ROCHE DIAGNOSTICS CK-MBRoche Diagnostics Corp.K961501ELECSYS CK-MBBoehringer Mannheim Corp.K950186CK-MB METHOD FOR THE TECHNICON IMMUNO 1(R) SYSTEM IN-VITRO DIAGNOSTIC SYSTEMMiles, 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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