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FDA 510(k)

ADENOTOMES

K-Number: K822262 · 1982-08-25

ApplicantKelleher Corp.
Decision Date1982-08-25
Product CodeKBH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ADENOTOMES is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-25 under 510(k) number K822262. The device is classified under product code KBH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADENOTOMES?

ADENOTOMES is a medical device that received FDA 510(k) clearance on 1982-08-25. The listed applicant is Kelleher Corp.. The 510(k) number is K822262.

When did ADENOTOMES receive FDA 510(k) clearance?

ADENOTOMES received FDA 510(k) clearance on 1982-08-25, under 510(k) number K822262.

Who is the listed applicant for ADENOTOMES?

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 ADENOTOMES?

The FDA product code for ADENOTOMES is KBH.

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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

View all 94 devices →

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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