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FDA 510(k)

ENT TREATMENT UNITS

K-Number: K822252 · 1982-11-22

ApplicantKelleher Corp.
Decision Date1982-11-22
Product CodeETF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ENT TREATMENT UNITS is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-11-22 under 510(k) number K822252. The device is classified under product code ETF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENT TREATMENT UNITS?

ENT TREATMENT UNITS is a medical device that received FDA 510(k) clearance on 1982-11-22. The listed applicant is Kelleher Corp.. The 510(k) number is K822252.

When did ENT TREATMENT UNITS receive FDA 510(k) clearance?

ENT TREATMENT UNITS received FDA 510(k) clearance on 1982-11-22, under 510(k) number K822252.

Who is the listed applicant for ENT TREATMENT UNITS?

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 ENT TREATMENT UNITS?

The FDA product code for ENT TREATMENT UNITS is ETF.

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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 UNITK823111NYSTYMOGRAPH ACCESSK822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDSK822017TYMPANOSTOMY TUBES & VARIOUS TYPES

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Related Devices (Code: ETF)

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.

K953457JEDMED SPECTRUM ENT CABINETJedmed Instrument Co.K945395PREMIER MIRROR WARMERPremier Dental Products Co.K932470LANGGASSE 90Happersberger Otopront GmbHK911901MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCEStortzK910781#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCESMidmark Corp.K910243MOBILE TREATMENT CARTJedmed Instrument Co.

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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