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)

DYNAMIC CRUCIATE TESTER

K-Number: K881876 · 1988-11-17

ApplicantDyonics, Inc.
Decision Date1988-11-17
Product CodeLYH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DYNAMIC CRUCIATE TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Dyonics, Inc.. It received FDA 510(k) clearance on 1988-11-17 under 510(k) number K881876. The device is classified under product code LYH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNAMIC CRUCIATE TESTER?

DYNAMIC CRUCIATE TESTER is a medical device that received FDA 510(k) clearance on 1988-11-17. The listed applicant is Dyonics, Inc.. The 510(k) number is K881876.

When did DYNAMIC CRUCIATE TESTER receive FDA 510(k) clearance?

DYNAMIC CRUCIATE TESTER received FDA 510(k) clearance on 1988-11-17, under 510(k) number K881876.

Who is the listed applicant for DYNAMIC CRUCIATE TESTER?

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

What is the FDA product code for DYNAMIC CRUCIATE TESTER?

The FDA product code for DYNAMIC CRUCIATE TESTER is LYH.

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 Dyonics, 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.

K900070MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEMK896416DYONICS SHOULDER PORTAL SYSTEMK893136SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTYK890665MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIESK894728DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFEK892062PS3500 ARTHROSCOPIC SURGICAL SYSTEM

View all 19 devices →

Related Devices (Code: LYH)

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.

K943197KT1000/S KNEE LIGAMENT ARTHROMETERMedmetric Corp.K942059KT2000 KNEE LIGAMENT ARTHROMETERMedmetric Corp.K834462GENUCOMFar Orthopedics, Inc.K812806KT-1000 DEVICEMedmetric 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.

↑