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FDA 510(k)

AGGREGOMETER, DUAL CHANNEL PLATELET

K-Number: K760159 · 1976-07-20

ApplicantChrono-Log Corp.
Decision Date1976-07-20
Product CodeJBX
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

AGGREGOMETER, DUAL CHANNEL PLATELET is the device name listed in this FDA 510(k) record. The listed applicant is Chrono-Log Corp.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760159. The device is classified under product code JBX. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGGREGOMETER, DUAL CHANNEL PLATELET?

AGGREGOMETER, DUAL CHANNEL PLATELET is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Chrono-Log Corp.. The 510(k) number is K760159.

When did AGGREGOMETER, DUAL CHANNEL PLATELET receive FDA 510(k) clearance?

AGGREGOMETER, DUAL CHANNEL PLATELET received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760159.

Who is the listed applicant for AGGREGOMETER, DUAL CHANNEL PLATELET?

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

What is the FDA product code for AGGREGOMETER, DUAL CHANNEL PLATELET?

The FDA product code for AGGREGOMETER, DUAL CHANNEL PLATELET is JBX.

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Other records listing Chrono-Log 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.

K161329Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channelK050265CHRONO-LOG WHOLE BLOOD LUMI-AGGREGOMETER, MODEL 700K032951CHRONO-LOG WHOLE BLOOD AGGREGOMETER, MODELS 591A AND 592AK962426CHRONO-LOG WHOLE BLOOD AGGREGOMETER (WBA) 591/592K945414RISTOCETIN COFACTOR ASSAY KITK940792AGGRO/LINK VW COFACTOR SOFTWARE

View all 16 devices →

Related Devices (Code: JBX)

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.

K932566AGGRO/LINK CONTROL SOFTWAREChrono-Log Corp.K912774ARACHIDONIC ACIDHelena LaboratoriesK881829PAT PLATELET AGGREGATION TESTStreck Laboratories, Inc.K862775ASSERACHROM B-TG KITAmerican Bioproducts Co.K851025AGGRO/LINK COMPUTER INTERFACEChrono-Log Corp.K850592PLATELET AGGREGATION REAGENTChrono-Log Corp.

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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