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FDA 510(k)

BONE RONGEUNS ENT & RELATED ITEMS

K-Number: K822007 · 1982-08-12

ApplicantKelleher Corp.
Decision Date1982-08-12
Product CodeJZA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BONE RONGEUNS ENT & RELATED ITEMS is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-12 under 510(k) number K822007. The device is classified under product code JZA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE RONGEUNS ENT & RELATED ITEMS?

BONE RONGEUNS ENT & RELATED ITEMS is a medical device that received FDA 510(k) clearance on 1982-08-12. The listed applicant is Kelleher Corp.. The 510(k) number is K822007.

When did BONE RONGEUNS ENT & RELATED ITEMS receive FDA 510(k) clearance?

BONE RONGEUNS ENT & RELATED ITEMS received FDA 510(k) clearance on 1982-08-12, under 510(k) number K822007.

Who is the listed applicant for BONE RONGEUNS ENT & RELATED ITEMS?

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 BONE RONGEUNS ENT & RELATED ITEMS?

The FDA product code for BONE RONGEUNS ENT & RELATED ITEMS is JZA.

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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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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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