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FDA 510(k)

STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE

K-Number: K950990 · 1996-01-19

ApplicantStoeckert Instrumente
Decision Date1996-01-19
Product CodeDTQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE is the device name listed in this FDA 510(k) record. The listed applicant is Stoeckert Instrumente. It received FDA 510(k) clearance on 1996-01-19 under 510(k) number K950990. 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 STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE?

STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE is a medical device that received FDA 510(k) clearance on 1996-01-19. The listed applicant is Stoeckert Instrumente. The 510(k) number is K950990.

When did STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE receive FDA 510(k) clearance?

STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE received FDA 510(k) clearance on 1996-01-19, under 510(k) number K950990.

Who is the listed applicant for STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE?

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

What is the FDA product code for STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE?

The FDA product code for STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE is DTQ.

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Other records listing Stoeckert Instrumente 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.

K002273STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAEK001961STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAEK002118STOCKERT COMPACT SYSTEM VERSION 2.0K992635INTERFACE MODULE IDDDK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSK982014STOCKERT COMPACT SYSTEM

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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

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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