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)

LAB-SITE(R) SAFETY CANNULA

K-Number: K933929 · 1993-12-07

ApplicantMigada, Ltd.
Decision Date1993-12-07
Product CodeCBF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LAB-SITE(R) SAFETY CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Migada, Ltd.. It received FDA 510(k) clearance on 1993-12-07 under 510(k) number K933929. The device is classified under product code CBF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAB-SITE(R) SAFETY CANNULA?

LAB-SITE(R) SAFETY CANNULA is a medical device that received FDA 510(k) clearance on 1993-12-07. The listed applicant is Migada, Ltd.. The 510(k) number is K933929.

When did LAB-SITE(R) SAFETY CANNULA receive FDA 510(k) clearance?

LAB-SITE(R) SAFETY CANNULA received FDA 510(k) clearance on 1993-12-07, under 510(k) number K933929.

Who is the listed applicant for LAB-SITE(R) SAFETY CANNULA?

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

What is the FDA product code for LAB-SITE(R) SAFETY CANNULA?

The FDA product code for LAB-SITE(R) SAFETY CANNULA is CBF.

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 Migada, Ltd. 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.

K943095IV TRANSFER SPIKEK902881LAB-SITE SAFETY NEEDLEK870016ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)K864453EMERGENCY & MILITARY INFUSION SYSTEMK863304PRESELECTED FLOW RATE I.V. SETK860952I.V. SET WITH AND WITHOUT AIR VENT

View all 15 devices →

Related Devices (Code: CBF)

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.

K240569FESL FINK Chamber; FEDL FINK Chamber; FETL FINK ChamberFink Engineering Pty, Ltd.K220290Revitalair 430+Us Hyperbaric NetworkK171899Revitalair 430FOxavita SrlK163109OxyHeal 4000 Multiplace Hyperbaric Chamber FamilyOxyheal Medical Systems, Inc.K152223Rectangular Multiplace Hyperbaric Chamber System Product Family with Touchscreen Control SystemOxyheal Medical Systems, Inc.K102831RSI 4200Reimers 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.

↑