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FDA 510(k)

EMERGENCY TRACHEOSTOMY INSTRUMENT SET

K-Number: K822618 · 1983-01-28

ApplicantKelleher Corp.
Decision Date1983-01-28
Product CodeLJW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EMERGENCY TRACHEOSTOMY INSTRUMENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1983-01-28 under 510(k) number K822618. The device is classified under product code LJW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERGENCY TRACHEOSTOMY INSTRUMENT SET?

EMERGENCY TRACHEOSTOMY INSTRUMENT SET is a medical device that received FDA 510(k) clearance on 1983-01-28. The listed applicant is Kelleher Corp.. The 510(k) number is K822618.

When did EMERGENCY TRACHEOSTOMY INSTRUMENT SET receive FDA 510(k) clearance?

EMERGENCY TRACHEOSTOMY INSTRUMENT SET received FDA 510(k) clearance on 1983-01-28, under 510(k) number K822618.

Who is the listed applicant for EMERGENCY TRACHEOSTOMY INSTRUMENT SET?

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

What is the FDA product code for EMERGENCY TRACHEOSTOMY INSTRUMENT SET?

The FDA product code for EMERGENCY TRACHEOSTOMY INSTRUMENT SET is LJW.

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Other records listing Kelleher 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.

K822268NAGASHIMA NS-III ELECTRONYSTAGMOGRAPHK823083ELECTROSURGICAL UNITK822252ENT TREATMENT UNITSK823111NYSTYMOGRAPH ACCESSK822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDSK822017TYMPANOSTOMY TUBES & VARIOUS TYPES

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Related Devices (Code: LJW)

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.

K933570RESOLUTION(TM) HIP STEMWrightmedicaltechnologyinc

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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