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)

PLASTIC BLUNT CANNULA

K-Number: K952976 · 1995-09-15

ApplicantMarquette Medical, Inc.
Decision Date1995-09-15
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLASTIC BLUNT CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Medical, Inc.. It received FDA 510(k) clearance on 1995-09-15 under 510(k) number K952976. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC BLUNT CANNULA?

PLASTIC BLUNT CANNULA is a medical device that received FDA 510(k) clearance on 1995-09-15. The listed applicant is Marquette Medical, Inc.. The 510(k) number is K952976.

When did PLASTIC BLUNT CANNULA receive FDA 510(k) clearance?

PLASTIC BLUNT CANNULA received FDA 510(k) clearance on 1995-09-15, under 510(k) number K952976.

Who is the listed applicant for PLASTIC BLUNT CANNULA?

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

What is the FDA product code for PLASTIC BLUNT CANNULA?

The FDA product code for PLASTIC BLUNT CANNULA is FPA.

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 Marquette Medical, 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.

K021471MARQUETTE HUBER TRAP SAFETY INFUSION SETK953008INFANT FEEDING TUBEK920537SUBCUTANEOUS INFUSION SETK9052184 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMPK9052194' LOW VOLUME IV EXTENSION SETK905374IV EXTENSION SETS WITH .22 MICRON FILTER

View all 17 devices →

Related Devices (Code: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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.

↑