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)

MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM

K-Number: K003090 · 2000-10-18

ApplicantMidmark Corp.
Decision Date2000-10-18
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 2000-10-18 under 510(k) number K003090. 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 MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM?

MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2000-10-18. The listed applicant is Midmark Corp.. The 510(k) number is K003090.

When did MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM receive FDA 510(k) clearance?

MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM received FDA 510(k) clearance on 2000-10-18, under 510(k) number K003090.

Who is the listed applicant for MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM?

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

What is the FDA product code for MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM?

The FDA product code for MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM 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

Other records listing Midmark Corp. 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.

K122643VANTAGE MODEL V5000, V5100, V5000C, V5100CK112380CLEARVISIONK090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERK023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERK992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZERK990189MODIFICATION OF: MIDMARK M-11 ULTRACLAVE STEAM STERILIZER

View all 31 devices →

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.

↑