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FDA 510(k)

PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE

K-Number: K881456 · 1988-10-14

ApplicantLaboratoire Ccd C/O Washington Regulatory Services
Decision Date1988-10-14
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE is the device name listed in this FDA 510(k) record. The listed applicant is Laboratoire Ccd C/O Washington Regulatory Services. It received FDA 510(k) clearance on 1988-10-14 under 510(k) number K881456. 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 PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE?

PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE is a medical device that received FDA 510(k) clearance on 1988-10-14. The listed applicant is Laboratoire Ccd C/O Washington Regulatory Services. The 510(k) number is K881456.

When did PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE receive FDA 510(k) clearance?

PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE received FDA 510(k) clearance on 1988-10-14, under 510(k) number K881456.

Who is the listed applicant for PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE?

The FDA 510(k) record lists Laboratoire Ccd C/O Washington Regulatory Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE?

The FDA product code for PIPELLE DE CORNIER ENDOMETRIAL 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.

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Other records listing Laboratoire Ccd C/O Washington Regulatory Services 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.

K890706CYTOBRUSHK884696RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SETK881220ENDOCYTE, DISPOSABLE ENDOMETRIAL SAMPLER

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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