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)

PROCEDURE READY TRAYS

K-Number: K884577 · 1989-08-01

ApplicantProfessional Medical Services
Decision Date1989-08-01
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

PROCEDURE READY TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Services. It received FDA 510(k) clearance on 1989-08-01 under 510(k) number K884577. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PROCEDURE READY TRAYS?

PROCEDURE READY TRAYS is a medical device that received FDA 510(k) clearance on 1989-08-01. The listed applicant is Professional Medical Services. The 510(k) number is K884577.

When did PROCEDURE READY TRAYS receive FDA 510(k) clearance?

PROCEDURE READY TRAYS received FDA 510(k) clearance on 1989-08-01, under 510(k) number K884577.

Who is the listed applicant for PROCEDURE READY TRAYS?

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

What is the FDA product code for PROCEDURE READY TRAYS?

The FDA product code for PROCEDURE READY TRAYS 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 Professional Medical Services 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.

K913094DISPOSABLE SLIDE VALVE MANIFOLDK910378PRESSURE MONITORING EXTENSION LINEK904508CONDOR ANALOG INFLATION SYRINGEK904954CONDOR DIGITAL INFLATION SYRINGEK902606RADIOPAQUE RULERK890471PMS ANGIO DRAPE

View all 19 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.

↑