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)

MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER

K-Number: K952652 · 1995-09-15

ApplicantMedscand (Usa), Inc.
Decision Date1995-09-15
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Medscand (Usa), Inc.. It received FDA 510(k) clearance on 1995-09-15 under 510(k) number K952652. 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 MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER?

MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER is a medical device that received FDA 510(k) clearance on 1995-09-15. The listed applicant is Medscand (Usa), Inc.. The 510(k) number is K952652.

When did MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER receive FDA 510(k) clearance?

MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER received FDA 510(k) clearance on 1995-09-15, under 510(k) number K952652.

Who is the listed applicant for MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER?

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

What is the FDA product code for MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER?

The FDA product code for MEDSCAND ENDORETTE ENDOMETRIAL SAMPLER 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

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.

↑