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FDA 510(k)

HEPARIN PUMP

K-Number: K761050 · 1976-12-30

ApplicantDws, Inc.
Decision Date1976-12-30
Product CodeFIR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HEPARIN PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Dws, Inc.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K761050. The device is classified under product code FIR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEPARIN PUMP?

HEPARIN PUMP is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is Dws, Inc.. The 510(k) number is K761050.

When did HEPARIN PUMP receive FDA 510(k) clearance?

HEPARIN PUMP received FDA 510(k) clearance on 1976-12-30, under 510(k) number K761050.

Who is the listed applicant for HEPARIN PUMP?

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

What is the FDA product code for HEPARIN PUMP?

The FDA product code for HEPARIN PUMP is FIR.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dws, 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.

K761051BI-FLOW NEEDLE

Related Devices (Code: FIR)

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.

K961137ATI PLASMA PUMP (PP-04)Apheresis Technologies, Inc.K831953INFUSION PUMPCryosan, Inc.K830818ASAHI BLOOD/PLASMA PUMP #ABP-01A &Parker Hannifin Corp.K821139SPS-SINGLE PATIENT SYSTEMExtracorporeal Medical Specialities, Inc.K780410BLOOD PUMP-MODE S10K3M Health Care, SarnsK771705RS-7800 MINIPUMPRenal Systems, 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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