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FDA 510(k)

PLATELET AGGREGATION REAGENTS

K-Number: K922800 · 1992-08-26

ApplicantChrono-Log Corp.
Decision Date1992-08-26
Product CodeGHR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PLATELET AGGREGATION REAGENTS 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 1992-08-26 under 510(k) number K922800. The device is classified under product code GHR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLATELET AGGREGATION REAGENTS?

PLATELET AGGREGATION REAGENTS is a medical device that received FDA 510(k) clearance on 1992-08-26. The listed applicant is Chrono-Log Corp.. The 510(k) number is K922800.

When did PLATELET AGGREGATION REAGENTS receive FDA 510(k) clearance?

PLATELET AGGREGATION REAGENTS received FDA 510(k) clearance on 1992-08-26, under 510(k) number K922800.

Who is the listed applicant for PLATELET AGGREGATION REAGENTS?

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 PLATELET AGGREGATION REAGENTS?

The FDA product code for PLATELET AGGREGATION REAGENTS is GHR.

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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

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Related Devices (Code: GHR)

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.

K061991PLATELETWORKS ARACHIDONIC ACID, MODEL PW-ACAHelena LaboratoriesK952252ADP REAGENT, MODIFIEDHelena LaboratoriesK910706COLLAGEN REAGENT CAT. NO. 5368Helena LaboratoriesK910800ADP REAGENTHelena LaboratoriesK910680EPINEPHRINE REAGENT, CAT. NO. 5367Helena LaboratoriesK910286PLATELET AGGREGATION REAGENTSMedical Diagnostic Technologies, 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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