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FDA 510(k)

TRACHEAL TUBE STYLET

K-Number: K902180 · 1990-07-19

ApplicantSims Surgical, Inc.
Decision Date1990-07-19
Product CodeBSR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRACHEAL TUBE STYLET is the device name listed in this FDA 510(k) record. The listed applicant is Sims Surgical, Inc.. It received FDA 510(k) clearance on 1990-07-19 under 510(k) number K902180. The device is classified under product code BSR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACHEAL TUBE STYLET?

TRACHEAL TUBE STYLET is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is Sims Surgical, Inc.. The 510(k) number is K902180.

When did TRACHEAL TUBE STYLET receive FDA 510(k) clearance?

TRACHEAL TUBE STYLET received FDA 510(k) clearance on 1990-07-19, under 510(k) number K902180.

Who is the listed applicant for TRACHEAL TUBE STYLET?

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

What is the FDA product code for TRACHEAL TUBE STYLET?

The FDA product code for TRACHEAL TUBE STYLET is BSR.

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 Sims Surgical, 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.

K902517NEUROSURGICAL HEADFRAME ACCESSORIESK902516NEW LENGTH SUGITA APPLIERS

Related Devices (Code: BSR)

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.

K162729Aintree Intubation Catheter, Arndt Airway Exchange Catheter Set, Cook Airway Exchange Catheter, and Cook Airway Exchange Catheter - Extra Firm With Soft TipCook IncorporatedK962361TRACHLIGHT STYLET AND TRACHEAL LIGHTWANDLaerdal Medical Corp.K954771TRACHLIGHT STYLET & TRACHEAL LIGHTWAND (ORIGINAL APPLICATION NAME: STYLETT & TRACHEAL LIGHTWAND)Laerdal Medical Corp.K943104MOLLOY INTUBATING STYLETTEMolloy Corp.K955238RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLERusch Intl.K953677LIGHTED FLEXGUIDE (MODIFICATION)Scientific Sales Intl., 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.

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