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)

DISPOSABLE VACUUM CURETTE

K-Number: K790032 · 1979-02-01

ApplicantBritish Marketing Ent., Ltd.
Decision Date1979-02-01
Product CodeHCY
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE VACUUM CURETTE is the device name listed in this FDA 510(k) record. The listed applicant is British Marketing Ent., Ltd.. It received FDA 510(k) clearance on 1979-02-01 under 510(k) number K790032. The device is classified under product code HCY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE VACUUM CURETTE?

DISPOSABLE VACUUM CURETTE is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is British Marketing Ent., Ltd.. The 510(k) number is K790032.

When did DISPOSABLE VACUUM CURETTE receive FDA 510(k) clearance?

DISPOSABLE VACUUM CURETTE received FDA 510(k) clearance on 1979-02-01, under 510(k) number K790032.

Who is the listed applicant for DISPOSABLE VACUUM CURETTE?

The FDA 510(k) record lists British Marketing Ent., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE VACUUM CURETTE?

The FDA product code for DISPOSABLE VACUUM CURETTE is HCY.

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 British Marketing Ent., Ltd. 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.

K782067DILATOR, MIZUTANI LAMINARIA TENT

Related Devices (Code: HCY)

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.

K980096OAC (OPTICAL ASPIRATING CURETTE)Imagyn Medical Technologies, Inc.K944238ENDOCYTE TMD.L. Nelson and Assoc., Inc.K935822PHASE I CURETTEPhase I Corp.K901442BAXTER D & C TRAYBaxter Healthcare CorpK890384UTERINE CURETTEKinetic Medical ProductsK881794IVORY FINDER SETIvory Instruments Co.

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.

↑