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FDA 510(k)

QUICKRATE REACTION RATE ANALYZER

K-Number: K780972 · 1978-08-14

ApplicantOlympus Corp.
Decision Date1978-08-14
Product CodeJJI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUICKRATE REACTION RATE ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1978-08-14 under 510(k) number K780972. The device is classified under product code JJI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKRATE REACTION RATE ANALYZER?

QUICKRATE REACTION RATE ANALYZER is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Olympus Corp.. The 510(k) number is K780972.

When did QUICKRATE REACTION RATE ANALYZER receive FDA 510(k) clearance?

QUICKRATE REACTION RATE ANALYZER received FDA 510(k) clearance on 1978-08-14, under 510(k) number K780972.

Who is the listed applicant for QUICKRATE REACTION RATE ANALYZER?

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

What is the FDA product code for QUICKRATE REACTION RATE ANALYZER?

The FDA product code for QUICKRATE REACTION RATE ANALYZER is JJI.

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Other records listing Olympus 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.

K915402EW-10 AND EW-20K933200OLYMPUS PBD STENTSK942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIESK931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESSK934835FLOVALK931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

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Related Devices (Code: JJI)

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.

K972024CODA AUTOMATED EIA ANALYZERBio-RadK944731ABBOTT IMX 2 ANALYZERAbbott LaboratoriesK931970ABBOTT IMX2 ANALYERAbbott LaboratoriesK930898RADIAS AUTOMATED IMMUNOASSAY SYSTEMBio-RadK790073ANALYZER, IMPACT 100Gilford Instrument Laboratories, Inc.K771591MINISTAT-S CHEMISTRY ANALYZERBiokinetix 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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