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)

KNOW-RECIRC

K-Number: K953551 · 1996-06-21

ApplicantH&H Control Systems
Decision Date1996-06-21
Product CodeMQS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KNOW-RECIRC is the device name listed in this FDA 510(k) record. The listed applicant is H&H Control Systems. It received FDA 510(k) clearance on 1996-06-21 under 510(k) number K953551. The device is classified under product code MQS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNOW-RECIRC?

KNOW-RECIRC is a medical device that received FDA 510(k) clearance on 1996-06-21. The listed applicant is H&H Control Systems. The 510(k) number is K953551.

When did KNOW-RECIRC receive FDA 510(k) clearance?

KNOW-RECIRC received FDA 510(k) clearance on 1996-06-21, under 510(k) number K953551.

Who is the listed applicant for KNOW-RECIRC?

The FDA 510(k) record lists H&H Control Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KNOW-RECIRC?

The FDA product code for KNOW-RECIRC is MQS.

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: MQS)

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.

K232283PhySoftAMS®Physician Software Systems, LLCK180410Dosis SAMDosis, Inc.K130579PHYSOFT AMSPhysicians Software Systems, LLCK042566VASC-ALERTVasc-Alert, Inc.K022963TRANSONIC SYRINGE WARMER, MODEL SYR-1000Transonic Systems, Inc.K021571TRANSONIC FLOW-QC SET MODEL ADT1010Transonic 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.

↑