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)

ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH)

K-Number: K900187 · 1990-05-01

ApplicantAdvance Medical Designs, Inc.
Decision Date1990-05-01
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH) is the device name listed in this FDA 510(k) record. The listed applicant is Advance Medical Designs, Inc.. It received FDA 510(k) clearance on 1990-05-01 under 510(k) number K900187. 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 ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH)?

ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH) is a medical device that received FDA 510(k) clearance on 1990-05-01. The listed applicant is Advance Medical Designs, Inc.. The 510(k) number is K900187.

When did ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH) receive FDA 510(k) clearance?

ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH) received FDA 510(k) clearance on 1990-05-01, under 510(k) number K900187.

Who is the listed applicant for ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH)?

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

What is the FDA product code for ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH)?

The FDA product code for ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH) 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 Advance Medical Designs, 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.

K223689Disposable Needle Guides and GridsK163050Advance Medical Designs, Inc. Sterile Ultrasound GelK053495EQUIPMENT SLUSH DRAPEK011265ULTRASOUND TRANSDUCER COVERK012168ADVANCE MEDICAL DESIGNS FLUID POUCHK011422SURGICAL DRAPES

View all 32 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.

↑