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FDA 510(k)

RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)

K-Number: K991895 · 1999-08-12

ApplicantRi Mos. S.R.L.
Decision Date1999-08-12
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217) is the device name listed in this FDA 510(k) record. The listed applicant is Ri Mos. S.R.L.. It received FDA 510(k) clearance on 1999-08-12 under 510(k) number K991895. 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 RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)?

RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217) is a medical device that received FDA 510(k) clearance on 1999-08-12. The listed applicant is Ri Mos. S.R.L.. The 510(k) number is K991895.

When did RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217) receive FDA 510(k) clearance?

RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217) received FDA 510(k) clearance on 1999-08-12, under 510(k) number K991895.

Who is the listed applicant for RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)?

The FDA 510(k) record lists Ri Mos. S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)?

The FDA product code for RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217) is HHK.

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Other records listing Ri Mos. S.R.L. 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.

K992926GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195)K991827GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102, 720103, 720179, 720227, 720043K983897CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G

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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