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FDA 510(k)

IEC CENTRA-7 CENTRIFUGE MODEL 2362

K-Number: K782124 · 1979-02-26

ApplicantDamon Corp.
Decision Date1979-02-26
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IEC CENTRA-7 CENTRIFUGE MODEL 2362 is the device name listed in this FDA 510(k) record. The listed applicant is Damon Corp.. It received FDA 510(k) clearance on 1979-02-26 under 510(k) number K782124. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IEC CENTRA-7 CENTRIFUGE MODEL 2362?

IEC CENTRA-7 CENTRIFUGE MODEL 2362 is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Damon Corp.. The 510(k) number is K782124.

When did IEC CENTRA-7 CENTRIFUGE MODEL 2362 receive FDA 510(k) clearance?

IEC CENTRA-7 CENTRIFUGE MODEL 2362 received FDA 510(k) clearance on 1979-02-26, under 510(k) number K782124.

Who is the listed applicant for IEC CENTRA-7 CENTRIFUGE MODEL 2362?

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

What is the FDA product code for IEC CENTRA-7 CENTRIFUGE MODEL 2362?

The FDA product code for IEC CENTRA-7 CENTRIFUGE MODEL 2362 is JQC.

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Other records listing Damon 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.

K874865DAMON D.E.T.E.C.T IMAGE ENHANCERK831826ADRENOCORTICOTROPIN RADIO-IMMUNOASSAYK820686LIQUISOL PROGESTERONE RADIOIMMUNOK802661LIQUISOL TESTOSTERONE RADIOIMM. TEST KITK790250LIQUISOL CORTISOL RIA TEST KITK781012RIA TEST KIT SYS. DAMON KIQUISOL FREE

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Related Devices (Code: JQC)

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.

K183205PureBMC SupraPhysiologic Concentrating System 30 mL System, PureBMC SupraPhysiologic Concentrating System 60 mL System, PureBMC SupraPhysiologic Concentrating System 120 mL SystemEmcyte CorporationK103340SMARTPREP2 BMAC SYSTEM, SMARTPREP PLATELET CONCENTRATION SYSTEMHarvest Technologies, Corp.K081345AXP PLATFORM MARROW XPRESS SYSTEM MODEL 8-5137, 8-5138, 8-5139, 8-5140 (PRIMARY)Thermogenesis Corp.K071934MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KITBiomet Manufacturing CorpK070666GENESISCS COMPONENT CONCENTRATING SYSTEMPerfusion Partners & Assoc., Inc.K052925SMARTPREP2 CENTRIFUGE SYSTEMHarvest Technologies, 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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