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FDA 510(k)

AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP

K-Number: K894794 · 1989-11-21

ApplicantVitaid, Ltd.
Decision Date1989-11-21
Product CodeKPM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Vitaid, Ltd.. It received FDA 510(k) clearance on 1989-11-21 under 510(k) number K894794. The device is classified under product code KPM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP?

AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP is a medical device that received FDA 510(k) clearance on 1989-11-21. The listed applicant is Vitaid, Ltd.. The 510(k) number is K894794.

When did AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP receive FDA 510(k) clearance?

AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP received FDA 510(k) clearance on 1989-11-21, under 510(k) number K894794.

Who is the listed applicant for AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP?

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

What is the FDA product code for AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP?

The FDA product code for AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP is KPM.

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Other records listing Vitaid, Ltd. 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.

K050803PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBESK932647WIRE REINFORCED ENDOTRACHEAL TUBEK901738SELFCATHK894883PHYCON ALL SILICONE BALLOON CATHETERK894669LASER SHIELDING TUBEK894337UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM

View all 7 devices →

Related Devices (Code: KPM)

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.

K231096Automatic Continuous Effusion Shunt (ACES) System ACES SystemPleural Dynamics, Inc.K170405BD Curve Ascites ShuntCare FusionK012235DENVER PLEURAL EFFUSION SHUNT AND DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBERDenver Biomedical, Inc.K011862DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNTDenver Biomedical, Inc.K011020DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBERDenver Biomedicals, Inc.K003451DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUBLED-VALVED ASCITES TDenver Biomedicals, Inc.

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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