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)

NOVA SAFE SCALP VEIN BLOOD COLLECTION SET

K-Number: K090502 · 2009-03-10

ApplicantU.S. Safety Syringes Co., Inc.
Decision Date2009-03-10
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NOVA SAFE SCALP VEIN BLOOD COLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Safety Syringes Co., Inc.. It received FDA 510(k) clearance on 2009-03-10 under 510(k) number K090502. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA SAFE SCALP VEIN BLOOD COLLECTION SET?

NOVA SAFE SCALP VEIN BLOOD COLLECTION SET is a medical device that received FDA 510(k) clearance on 2009-03-10. The listed applicant is U.S. Safety Syringes Co., Inc.. The 510(k) number is K090502.

When did NOVA SAFE SCALP VEIN BLOOD COLLECTION SET receive FDA 510(k) clearance?

NOVA SAFE SCALP VEIN BLOOD COLLECTION SET received FDA 510(k) clearance on 2009-03-10, under 510(k) number K090502.

Who is the listed applicant for NOVA SAFE SCALP VEIN BLOOD COLLECTION SET?

The FDA 510(k) record lists U.S. Safety Syringes Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOVA SAFE SCALP VEIN BLOOD COLLECTION SET?

The FDA product code for NOVA SAFE SCALP VEIN BLOOD COLLECTION SET is FOZ.

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 U.S. Safety Syringes Co., 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.

K090122NUOVOGUARDK083454NUOVOCATHK080665NOVOLETK080660IV ADMINISTRATION SETK003381SHIELDING NEEDLE HOLDERK990831SUPERGUARD SAFETY SYRINGE

View all 7 devices →

Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy 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.

↑