FDA 510(k)

CURITY FIBEROPTIC INTUBATING AIRWAY

K-Number: K855137 · 1986-03-11

Decision Date1986-03-11

Product CodeCAE

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CURITY FIBEROPTIC INTUBATING AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1986-03-11 under 510(k) number K855137. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY FIBEROPTIC INTUBATING AIRWAY?

CURITY FIBEROPTIC INTUBATING AIRWAY is a medical device that received FDA 510(k) clearance on 1986-03-11. The listed applicant is The Kendal Co.. The 510(k) number is K855137.

When did CURITY FIBEROPTIC INTUBATING AIRWAY receive FDA 510(k) clearance?

CURITY FIBEROPTIC INTUBATING AIRWAY received FDA 510(k) clearance on 1986-03-11, under 510(k) number K855137.

Who is the listed applicant for CURITY FIBEROPTIC INTUBATING AIRWAY?

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

What is the FDA product code for CURITY FIBEROPTIC INTUBATING AIRWAY?

The FDA product code for CURITY FIBEROPTIC INTUBATING AIRWAY is CAE.

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Other records listing The Kendal Co. as applicant

K000087MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR K990500KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946C K991758MONOJECT INSULIN SYRINGE K970969KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET K951488KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP K942664KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM

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Related Devices (Code: CAE)

K033189KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305King Systems Corp.K033186KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205King Systems Corp.K021634KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105King Systems Corp.K955721CUFFED OROPHARYNGEAL AIRWAY (COPA)Mallinckrodt Medical K960240RUSCH OPTOSAFERusch Intl.K950613KEISEIKeisei (Usa) Co., Ltd.

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.