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)

MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS

K-Number: K924875 · 1994-06-30

ApplicantSynectics-Dantec
Decision Date1994-06-30
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS is the device name listed in this FDA 510(k) record. The listed applicant is Synectics-Dantec. It received FDA 510(k) clearance on 1994-06-30 under 510(k) number K924875. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS?

MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS is a medical device that received FDA 510(k) clearance on 1994-06-30. The listed applicant is Synectics-Dantec. The 510(k) number is K924875.

When did MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS receive FDA 510(k) clearance?

MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS received FDA 510(k) clearance on 1994-06-30, under 510(k) number K924875.

Who is the listed applicant for MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS?

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

What is the FDA product code for MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS?

The FDA product code for MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS is BZQ.

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 Synectics-Dantec 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.

K961346PH ANALYSIS MODULEK925405ZINETICS COMPOSITE SENSOR PROBE W/INTERNAL REF.K914793MONOCRYSTANT PH/LES CATHETER, MODIFICATIONK924383SYNECTICS LIBERTY SYSTEM, PC POLYGRAF/POLYGRAM UROK913817MONOCRYSTANT PH-REFERENCE CATHETER, MODIFICATIONK914624PH METER, MODIFICATION

View all 19 devices →

Related Devices (Code: BZQ)

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.

K253274BedDot (G1)Intelligent Dots, LLCK251326Respiration Rate algorithmEdwards Lifesciences, LLCK250093Linshom Continuous Predictive Respiratory Monitoring System (CPRMS)Linshom Medical, Inc.K250934Respiree Cardio- Respiratory Monitor SystemRespiree Pte, Ltd.K243183RTMsense Respiratory Monitoring SystemRtm Vital Signs, LLCK243966FaceHeart Vitals Software Development Kit (FH vitals SDK-RR)Faceheart Corp.

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.

↑