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)

DRESSING CHANGE TRAYS

K-Number: K833126 · 1984-01-27

ApplicantIntermed, Inc.
Decision Date1984-01-27
Product Code
DecisionSubstantially Equivalent

Device Summary

DRESSING CHANGE TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Intermed, Inc.. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K833126. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRESSING CHANGE TRAYS?

DRESSING CHANGE TRAYS is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Intermed, Inc.. The 510(k) number is K833126.

When did DRESSING CHANGE TRAYS receive FDA 510(k) clearance?

DRESSING CHANGE TRAYS received FDA 510(k) clearance on 1984-01-27, under 510(k) number K833126.

Who is the listed applicant for DRESSING CHANGE TRAYS?

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

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 Intermed, 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.

K900857NON STERILE PARENTERAL SUPPLY KITK842166INTERMED, INS STERILE WATER/SALINEK833574PERCUTANEOUS SHEATH INTRODUCER TRAYSK833573CENTRAL VEIN CATH. TRAY CC-20-1420K833139ACUTE HEMODIALYSIS TRAYSK833059SUCTION CATHETER TRAYS

View all 16 devices →

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.

↑