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FDA 510(k)

LARYNGEAL SPATULAS

K-Number: K822259 · 1982-10-22

ApplicantKelleher Corp.
Decision Date1982-10-22
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LARYNGEAL SPATULAS is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-10-22 under 510(k) number K822259. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARYNGEAL SPATULAS?

LARYNGEAL SPATULAS is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is Kelleher Corp.. The 510(k) number is K822259.

When did LARYNGEAL SPATULAS receive FDA 510(k) clearance?

LARYNGEAL SPATULAS received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822259.

Who is the listed applicant for LARYNGEAL SPATULAS?

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 LARYNGEAL SPATULAS?

The FDA product code for LARYNGEAL SPATULAS is EQH.

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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.

K822618EMERGENCY TRACHEOSTOMY INSTRUMENT SETK822268NAGASHIMA NS-III ELECTRONYSTAGMOGRAPHK823083ELECTROSURGICAL UNITK822252ENT TREATMENT UNITSK823111NYSTYMOGRAPH ACCESSK822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS

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Related Devices (Code: EQH)

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.

K945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTWells Johnson Co.K954184JED-LIGHT FIBEROPTIC LIGHT SOURCEJedmed Instrument Co.K951829COLD LIGHT SOURCE LOS 150Laser-Optik-Systeme GmbH & Co. KGK932771BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCEXomed-Treace, Inc.K941661GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHTGm Engineering, Inc.K941662GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHTGm Engineering, 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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