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FDA 510(k)

STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE

K-Number: K861714 · 1986-07-16

ApplicantShiley, Inc.
Decision Date1986-07-16
Product CodeDWB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1986-07-16 under 510(k) number K861714. The device is classified under product code DWB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE?

STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE is a medical device that received FDA 510(k) clearance on 1986-07-16. The listed applicant is Shiley, Inc.. The 510(k) number is K861714.

When did STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE receive FDA 510(k) clearance?

STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE received FDA 510(k) clearance on 1986-07-16, under 510(k) number K861714.

Who is the listed applicant for STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE?

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

What is the FDA product code for STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE?

The FDA product code for STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE is DWB.

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Other records listing Shiley, Inc. 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.

K920594SHILEY PERFUSION TUBING SETSK910991SHILEY THERAPEUTIC AUTOTRANSFUSION SYSTEMK911876SHILEY PLEXUS(R) VENOUS RESERVOIR, PVR1200K910923BCD ADVANCEDK901548BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GASK903435SHILEY SPECIALIZED TRACHEOSTOMY TUBE

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Related Devices (Code: DWB)

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.

K162843Small (4) Roller Pump for the Terumo Advanced Perfusion System 1, Large (6) Roller Pump for the Terumo Advanced Perfusion System 1Terumo Cardiovascular Systems CorporationK131618LARGE (6) ROLLER PUMP FOR TERUMO ADVANCED PERFUSION SYSTEM 1; LARGE (6) ROLLER PUMP FOR TERUMO ADVANCED PERFUSION SYSTTerumo Cardiovascular Systems CorporationK112587ADVANCED PERFUSION SYSTEM 1 (APS1) TUBE CLAMP ASSEMBLY, ROLLER PUMP 6 INCH CLASSIC COLOR,Terumo Cardiovascular Systems Corp.K973237CSS-CARDIOPLEGIA SAFETY SYSTEMMedtronic Bio-Medicus, Inc.K972321S3 MAST PUMPStoeckert InstrumenteK971520S3 CYCLIC RPM CONTROLStoeckert Instrumente

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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