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)

THE PANPAC SUCTION CURETTE

K-Number: K092982 · 2010-07-26

ApplicantPanpac Medical Corporation
Decision Date2010-07-26
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE PANPAC SUCTION CURETTE is the device name listed in this FDA 510(k) record. The listed applicant is Panpac Medical Corporation. It received FDA 510(k) clearance on 2010-07-26 under 510(k) number K092982. 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 THE PANPAC SUCTION CURETTE?

THE PANPAC SUCTION CURETTE is a medical device that received FDA 510(k) clearance on 2010-07-26. The listed applicant is Panpac Medical Corporation. The 510(k) number is K092982.

When did THE PANPAC SUCTION CURETTE receive FDA 510(k) clearance?

THE PANPAC SUCTION CURETTE received FDA 510(k) clearance on 2010-07-26, under 510(k) number K092982.

Who is the listed applicant for THE PANPAC SUCTION CURETTE?

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

What is the FDA product code for THE PANPAC SUCTION CURETTE?

The FDA product code for THE PANPAC SUCTION CURETTE 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 Panpac Medical Corporation 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.

K173351Panpac Flexi Shelf PessaryK161106PANPAC DISPOSABLE VACUUM CURETTESK153422Panpac Disposable Pessary Fitting SetK130273PANPAC VAGINAL DILATORSK102898BELLOTA SONOHYSTEROGRAPHY CATHETER WITH CERVICAL CONE, BELLOTA SONOHYSTEROGRAPHY CATHETER WITHOUT CERVICAL CONEK092981PANPAC VAGINAL PESSARY

View all 10 devices →

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.K051294FEMTEST ENDOMETRIAL SUCTION CURETTE, MODEL FT-1Femspec LLC

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.

↑