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FDA 510(k)

PIONEER PRO-PUMP DUAL CONTROL

K-Number: K914241 · 1992-03-04

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

Device Summary

PIONEER PRO-PUMP DUAL CONTROL 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 K914241. 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 DUAL CONTROL?

PIONEER PRO-PUMP DUAL CONTROL 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 K914241.

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

PIONEER PRO-PUMP DUAL CONTROL received FDA 510(k) clearance on 1992-03-04, under 510(k) number K914241.

Who is the listed applicant for PIONEER PRO-PUMP DUAL CONTROL?

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 DUAL CONTROL?

The FDA product code for PIONEER PRO-PUMP DUAL CONTROL 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.

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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.

K914220PIONEER PRO-PUMP

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.

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