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)

TRIDENT DRAPE SUPPORT

K-Number: K895011 · 1989-09-15

ApplicantTrident Medical Products, Inc.
Decision Date1989-09-15
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRIDENT DRAPE SUPPORT is the device name listed in this FDA 510(k) record. The listed applicant is Trident Medical Products, Inc.. It received FDA 510(k) clearance on 1989-09-15 under 510(k) number K895011. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIDENT DRAPE SUPPORT?

TRIDENT DRAPE SUPPORT is a medical device that received FDA 510(k) clearance on 1989-09-15. The listed applicant is Trident Medical Products, Inc.. The 510(k) number is K895011.

When did TRIDENT DRAPE SUPPORT receive FDA 510(k) clearance?

TRIDENT DRAPE SUPPORT received FDA 510(k) clearance on 1989-09-15, under 510(k) number K895011.

Who is the listed applicant for TRIDENT DRAPE SUPPORT?

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

What is the FDA product code for TRIDENT DRAPE SUPPORT?

The FDA product code for TRIDENT DRAPE SUPPORT is KKX.

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 Trident Medical Products, 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.

K894720UNIVERSAL EYESHIELDK894724SAFE-EDGE EYESHIELD

Related Devices (Code: KKX)

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.

K230645BeneHold™ Surgical Incise Drape with CHG antimicrobial IIAvery Dennison Medical , Ltd.K2225783M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)3M CompanyK202208BeneHold Surgical Incise Drape with CHG antimicrobialAvery Dennison Belgie BvbaK200238ControlRad Sterile CoverControlrad, Inc.K163556MediClear PreOpCovalontechnologies, Inc.K130404TIBURON SURGICAL DRAPECardinal Health200, LLC

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.

↑