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)

COMPACT PLUS - EXTREME - PERFECT PLUS

K-Number: K052574 · 2006-07-17

ApplicantJ.O. Suarez & Cia, Ltda
Decision Date2006-07-17
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMPACT PLUS - EXTREME - PERFECT PLUS is the device name listed in this FDA 510(k) record. The listed applicant is J.O. Suarez & Cia, Ltda. It received FDA 510(k) clearance on 2006-07-17 under 510(k) number K052574. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPACT PLUS - EXTREME - PERFECT PLUS?

COMPACT PLUS - EXTREME - PERFECT PLUS is a medical device that received FDA 510(k) clearance on 2006-07-17. The listed applicant is J.O. Suarez & Cia, Ltda. The 510(k) number is K052574.

When did COMPACT PLUS - EXTREME - PERFECT PLUS receive FDA 510(k) clearance?

COMPACT PLUS - EXTREME - PERFECT PLUS received FDA 510(k) clearance on 2006-07-17, under 510(k) number K052574.

Who is the listed applicant for COMPACT PLUS - EXTREME - PERFECT PLUS?

The FDA 510(k) record lists J.O. Suarez & Cia, Ltda as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPACT PLUS - EXTREME - PERFECT PLUS?

The FDA product code for COMPACT PLUS - EXTREME - PERFECT PLUS is EIA.

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: EIA)

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.

K251544Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)Lakong Medical Devices Co., Ltd.K251626Midmark Dental Delivery SystemMidmark CorporationK251491K5 Cart, K5 Mount, K5 SwingOsstem Implant Company., Ltd. Chair BusinessK243130Integral Dental UnitGuangdong Yadeng Medical Apparatus Co., Ltd.,K242611Integral Dental UnitsMipont Medical Equipment Co., Ltd.K250473Dental Delivery System Series 5 and Dental Delivery System Series 5 PlusDci International, LLC

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.

↑