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FDA 510(k)

BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP

K-Number: K802230 · 1980-12-22

ApplicantCardio Med Supplies, Inc.
Decision Date1980-12-22
Product CodeFIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Med Supplies, Inc.. It received FDA 510(k) clearance on 1980-12-22 under 510(k) number K802230. The device is classified under product code FIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP?

BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Cardio Med Supplies, Inc.. The 510(k) number is K802230.

When did BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP receive FDA 510(k) clearance?

BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP received FDA 510(k) clearance on 1980-12-22, under 510(k) number K802230.

Who is the listed applicant for BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP?

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

What is the FDA product code for BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP?

The FDA product code for BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP is FIF.

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 Cardio Med Supplies, 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.

K080174PHLEBOTOMY BAG WITH VALVE & 17G X 1, MODEL CM-PH17X1B, CM-PH17X1CK04267214F DUAL FLOATING DIALYSIS CATHETER/TRAYK021080NONCOR INFUSION SETS; NONCOR PORT INFUSION SETSK833112TUBING FOR CARDIOPULMONARY BYPASS

Related Devices (Code: FIF)

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.

K8732798810 PUMP-PUMP SINGLE NEEDLE DEVICECd Medical, Inc.K820173COBE SINGLE-NEEDLE CONTROLLER #18-756Cobe Laboratories, Inc.K801967MEDCOMP FEMORAL VEIN CATHETERMedical Components, Inc.K792174MODEL DM 353 & DM-353-L SINGLE NEEDLEExtracorporeal Medical Specialities, Inc.K772147GW 35 GUIDE WIRESorensen Research

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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