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)

TREBAY IRRGATED CUTTER BLADE

K-Number: K951526 · 1995-05-12

ApplicantTrebay Medical Corp.
Decision Date1995-05-12
Product CodeEQJ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TREBAY IRRGATED CUTTER BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Trebay Medical Corp.. It received FDA 510(k) clearance on 1995-05-12 under 510(k) number K951526. The device is classified under product code EQJ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREBAY IRRGATED CUTTER BLADE?

TREBAY IRRGATED CUTTER BLADE is a medical device that received FDA 510(k) clearance on 1995-05-12. The listed applicant is Trebay Medical Corp.. The 510(k) number is K951526.

When did TREBAY IRRGATED CUTTER BLADE receive FDA 510(k) clearance?

TREBAY IRRGATED CUTTER BLADE received FDA 510(k) clearance on 1995-05-12, under 510(k) number K951526.

Who is the listed applicant for TREBAY IRRGATED CUTTER BLADE?

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

What is the FDA product code for TREBAY IRRGATED CUTTER BLADE?

The FDA product code for TREBAY IRRGATED CUTTER BLADE is EQJ.

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 Trebay Medical Corp. 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.

K955704TREBAY MICRODEBRIDER SYSTEMK955294SOF - ABRASION BURK955560TREBAY SCOPE IRRIGATED CLEARING SLEEVEK955447TYMPANOSTOMY TUBEK954912TREBAY IRRIGATED CUTTER BLADE (MODIFICATION)K954795AT2 & DOYLE STYLE (C-FLEX) VENT TUBES

View all 14 devices →

Related Devices (Code: EQJ)

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.

K161514Precision Thin Reciprocating Blade, 0.010in.Stryker CorporationK041985XPS CURVED BURMedtronic Xomed, Inc.K974232ESSENTIAL SHAVER SYSTEMGyrus Ent LLCK960853ACE SYSTEMXomed, Inc.K955704TREBAY MICRODEBRIDER SYSTEMTrebay Medical Corp.K955294SOF - ABRASION BURTrebay Medical Corp.

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.

↑