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FDA 510(k)

MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP

K-Number: K890904 · 1989-04-12

ApplicantShiley, Inc.
Decision Date1989-04-12
Product CodeDWB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1989-04-12 under 510(k) number K890904. 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 MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP?

MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP is a medical device that received FDA 510(k) clearance on 1989-04-12. The listed applicant is Shiley, Inc.. The 510(k) number is K890904.

When did MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP receive FDA 510(k) clearance?

MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP received FDA 510(k) clearance on 1989-04-12, under 510(k) number K890904.

Who is the listed applicant for MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP?

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 MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP?

The FDA product code for MODIFIED STOCKERT-SHILEY CAPS MULTI. ROLLER PUMP 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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