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)

ADAIR/VERESS NEEDLE INTRODUCER SET

K-Number: K930568 · 1993-07-22

ApplicantMedical Dynamics, Inc.
Decision Date1993-07-22
Product CodeGCB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADAIR/VERESS NEEDLE INTRODUCER SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Dynamics, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K930568. The device is classified under product code GCB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAIR/VERESS NEEDLE INTRODUCER SET?

ADAIR/VERESS NEEDLE INTRODUCER SET is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Medical Dynamics, Inc.. The 510(k) number is K930568.

When did ADAIR/VERESS NEEDLE INTRODUCER SET receive FDA 510(k) clearance?

ADAIR/VERESS NEEDLE INTRODUCER SET received FDA 510(k) clearance on 1993-07-22, under 510(k) number K930568.

Who is the listed applicant for ADAIR/VERESS NEEDLE INTRODUCER SET?

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

What is the FDA product code for ADAIR/VERESS NEEDLE INTRODUCER SET?

The FDA product code for ADAIR/VERESS NEEDLE INTRODUCER SET is GCB.

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 Medical Dynamics, 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.

K974542TRUE VISION, TRUE VISION IIK921294VIDEO ENDOSCOPE-RIGID MODIFICATIONK934682SURGICAL VIDEO CAMERA AND ACCESSORIESK915538OVER THE WIRE STONE BASKETK914315OPTICAL CATHETER INTRODUCER SETS, MODIFICATIONK913986CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM

View all 18 devices →

Related Devices (Code: GCB)

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.

K974146PARACENTESIS CATHETER DEVICEAllegiance Healthcare Corp.K923028TURKEL PNEUMOTHORAX KITSymbiosis Corp.K900374ADAIR/VERESS NEEDLE INTRODUCER SETMedical Dynamics, Inc.K854327SUBCUTANEOUS TUNNELING NEEDLES & HANDLESConcord Laboratories, Inc.K852428MANAN EPIDURAL NEEDLEManan Manufacturing Co., Inc.K780896NEEDLES, DESIGN CHANGE, IV CATHETERSJelco Laboratories

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.

↑