TRIDENT #2001

Electrosurgical, Cutting & Coagulation & Accessories

TRIDENT SURGICAL CORP.

The following data is part of a premarket notification filed by Trident Surgical Corp. with the FDA for Trident #2001.

Pre-market Notification Details

Device IDK812769
510k NumberK812769
Device Name:TRIDENT #2001
ClassificationElectrosurgical, Cutting & Coagulation & Accessories
Applicant TRIDENT SURGICAL CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGEI  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-10-05
Decision Date1981-11-06

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.