Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PIONEER PRO-PUMP

K-Number: K914220 · 1992-03-04

ApplicantPioneer Medical, Inc.
Decision Date1992-03-04
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PIONEER PRO-PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Medical, Inc.. It received FDA 510(k) clearance on 1992-03-04 under 510(k) number K914220. The device is classified under product code HHK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIONEER PRO-PUMP?

PIONEER PRO-PUMP is a medical device that received FDA 510(k) clearance on 1992-03-04. The listed applicant is Pioneer Medical, Inc.. The 510(k) number is K914220.

When did PIONEER PRO-PUMP receive FDA 510(k) clearance?

PIONEER PRO-PUMP received FDA 510(k) clearance on 1992-03-04, under 510(k) number K914220.

Who is the listed applicant for PIONEER PRO-PUMP?

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

What is the FDA product code for PIONEER PRO-PUMP?

The FDA product code for PIONEER PRO-PUMP is HHK.

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 Pioneer Medical, 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.

K914241PIONEER PRO-PUMP DUAL CONTROL

Related Devices (Code: HHK)

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.

K251882Uterine Aspiration SetGcmedica Enterprise Ltd.(Wuxi)K240434RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)Li Medical Corporation , Ltd.K201952CrossGlide ETS PlusCrossbay MedicalK192534CrossBay Endometrial Tissue Sampler (ETS)Crossbay MedicalK102847DISPOSABLE ENDOMETRIAL SUCTION CURETTEJiangsu Suyun Medical Materials Co., Ltd.K092982THE PANPAC SUCTION CURETTEPanpac Medical Corporation

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.

↑