FDA 510(k)

PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS

K-Number: K932711 · 1993-07-23

Decision Date1993-07-23

Product CodeBTR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS is the device name listed in this FDA 510(k) record. The listed applicant is Precision Med Products, Ltd.. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K932711. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS?

PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Precision Med Products, Ltd.. The 510(k) number is K932711.

When did PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS receive FDA 510(k) clearance?

PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS received FDA 510(k) clearance on 1993-07-23, under 510(k) number K932711.

Who is the listed applicant for PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS?

The FDA 510(k) record lists Precision Med Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS?

The FDA product code for PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS is BTR.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Precision Med Products, Ltd. as applicant

K932710GAS SAMPLING LINES AND CONNECTORS K932706PRECISION MED PRODUCTS LTD. VENTILATOR HOSE K932707ADULT ANESTHESIA BREATHING CIRCUIT K932708PRECISION MED PRODUCTS LTD MAPLESON D CIRCUITS K932709PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM K932489PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR.

View all 16 devices →

Related Devices (Code: BTR)

K251794Tenax® Laser Resistant Endotracheal TubeBryan Medical, Inc.K253437Spiro-VISTASpiro Robotics K250173Shiley™ Oral RAE Tracheal Tube Cuffless, Murphy Eye (113-XX) Shiley™ Nasal RAE Tracheal Tube Cuffless, Murphy Eye (114-XX) Shiley™ Oral RAE Tracheal Tube Cuffed, Murphy Eye (115-XX) Shiley™ Oral RAE Tracheal Tube with TaperGuard™ Cuff, Murphy Eye (115-XXOR) Shiley™ Nasal RAE Tracheal Tube with TaperGuard™ Cuff, Murphy Eye (119-XXNR)Covidien, LLC K243785Shiley™ Oral/Nasal Tracheal Tube with TaperGuard™ Cuff Reinforced, Murphy Eye Shiley™ Tracheal Tube TaperGuard™ Cuff Reinforced with Stylet Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced, Murphy Eye Shiley™ Oral/Nasal Tracheal Tube Cuffless ReinforcedCovidien, LLC K243579AeroJet Ventilation CatheterPipeline Medical Products, LLC K251499Frova Intubating Introducer (C-CAE-14.0-70-FII); Frova Intubating Introducer (C-CAE-14.0-70-FI); Frova Intubating Introducer (C-CAE-14.0-70-FIC); Frova Intubating Introducer (C-CAE-14.0-70-FIC-SPOPS)William Cook Europe Aps

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.