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FDA 510(k)

CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE

K-Number: K851615 · 1985-06-19

ApplicantCentrimed Corp.
Decision Date1985-06-19
Product CodeDTQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE is the device name listed in this FDA 510(k) record. The listed applicant is Centrimed Corp.. It received FDA 510(k) clearance on 1985-06-19 under 510(k) number K851615. The device is classified under product code DTQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE?

CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE is a medical device that received FDA 510(k) clearance on 1985-06-19. The listed applicant is Centrimed Corp.. The 510(k) number is K851615.

When did CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE receive FDA 510(k) clearance?

CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE received FDA 510(k) clearance on 1985-06-19, under 510(k) number K851615.

Who is the listed applicant for CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE?

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

What is the FDA product code for CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE?

The FDA product code for CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE is DTQ.

Related Clinical Trials

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.

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Other records listing Centrimed 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.

K851613CENTRIMED SYSTEM 1 W/SYSTEM 1 ADAPTERK851614CENTRIMED SYSTEM 1 W/24 VOLT BATTERY POWER SUPPLYK842007CENTRIMED SYSTEM 1

Related Devices (Code: DTQ)

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.

K232291Essenz HLM, Essenz ILBMLivanova Deutschland, GmbHK221895Terumo Advanced Perfusion System 1Terumo Cardiovascular Systems CorporationK221373Essenz HLMLivanova Deutschland, GmbHK210130Stockert S5 SystemLivanova Deutschland, GmbHK202125Century Perfusion SystemCentury Hlm, LLCK190282Quantum Smart Occluder LH (left-hand), Quantum Smart Occluder LH (right-hand)Spectrum Medical , Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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