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)

RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT

K-Number: K852749 · 1985-09-10

ApplicantMesa Medical, Inc.
Decision Date1985-09-10
Product CodeFKQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT is the device name listed in this FDA 510(k) record. The listed applicant is Mesa Medical, Inc.. It received FDA 510(k) clearance on 1985-09-10 under 510(k) number K852749. The device is classified under product code FKQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT?

RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT is a medical device that received FDA 510(k) clearance on 1985-09-10. The listed applicant is Mesa Medical, Inc.. The 510(k) number is K852749.

When did RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT receive FDA 510(k) clearance?

RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT received FDA 510(k) clearance on 1985-09-10, under 510(k) number K852749.

Who is the listed applicant for RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT?

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

What is the FDA product code for RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT?

The FDA product code for RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT is FKQ.

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 Mesa Medical, Inc. 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.

K92521090DX MULTITEST METER, MODIFICATIONK882032MODEL 90DX MULTITEST METERK870811MODEL 102 PH METERK843520WAREXIN RECOMMENDED ALTERNATIVE DIALYZK834447ECHO MM1000K821383ECHO, MODEL MM-1000

View all 7 devices →

Related Devices (Code: FKQ)

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.

K052764DIACAP ULTRA DIALYSIS FLUID FILTERB. Braun Medizintechnologie GmbHK893612TWO TANK DISSOLUTION MODULENational Medical Care, Medical Products Div., Inc.K874084MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDMNational Medical Care, Medical Products Div., Inc.K873421KAWASUMI A.V. FISTULA SETKawasumi Laboratories Co., Ltd.K870889ACID FUCHSIN SOLUTIONSD.R.G. Scientific IndustriesK861730ACTRIL FOR KIDNEY MACHINE DISINFECTANTRenal Systems, 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.

↑