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FDA 510(k)

FEMECC ENDOCERVICAL CURETTE

K-Number: K060320 · 2006-07-28

ApplicantFemspec LLC
Decision Date2006-07-28
Product CodePCF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FEMECC ENDOCERVICAL CURETTE is the device name listed in this FDA 510(k) record. The listed applicant is Femspec LLC. It received FDA 510(k) clearance on 2006-07-28 under 510(k) number K060320. The device is classified under product code PCF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMECC ENDOCERVICAL CURETTE?

FEMECC ENDOCERVICAL CURETTE is a medical device that received FDA 510(k) clearance on 2006-07-28. The listed applicant is Femspec LLC. The 510(k) number is K060320.

When did FEMECC ENDOCERVICAL CURETTE receive FDA 510(k) clearance?

FEMECC ENDOCERVICAL CURETTE received FDA 510(k) clearance on 2006-07-28, under 510(k) number K060320.

Who is the listed applicant for FEMECC ENDOCERVICAL CURETTE?

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

What is the FDA product code for FEMECC ENDOCERVICAL CURETTE?

The FDA product code for FEMECC ENDOCERVICAL CURETTE is PCF.

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 Femspec LLC 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.

K052192FEMSPCE-S DISPOSABLE STERILE VAGINAL SPECULUM, MODEL ST-IK051294FEMTEST ENDOMETRIAL SUCTION CURETTE, MODEL FT-1K041757FEMSPEC DISPOSABLE VAGINAL SPECULUM

Related Devices (Code: PCF)

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.

K122658FEMCERV ENDOCERVICAL SAMPLER MODEL 3 SIZES: REF FCV-013, REF FCV-011, REF FCV-009Femasys, Inc.K882606EURO-MED ENDO-CURETTEBuckman Co., Inc.K882404KEVOR-CURETTEEuro-Med Intl.K860796DISPO-URETTERoland J. Zwick, Inc.

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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