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FDA 510(k)

MICROSURGICAL EAR PICKS

K-Number: K822176 · 1982-08-16

ApplicantKelleher Corp.
Decision Date1982-08-16
Product CodeJYT
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MICROSURGICAL EAR PICKS is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-16 under 510(k) number K822176. The device is classified under product code JYT. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSURGICAL EAR PICKS?

MICROSURGICAL EAR PICKS is a medical device that received FDA 510(k) clearance on 1982-08-16. The listed applicant is Kelleher Corp.. The 510(k) number is K822176.

When did MICROSURGICAL EAR PICKS receive FDA 510(k) clearance?

MICROSURGICAL EAR PICKS received FDA 510(k) clearance on 1982-08-16, under 510(k) number K822176.

Who is the listed applicant for MICROSURGICAL EAR PICKS?

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 MICROSURGICAL EAR PICKS?

The FDA product code for MICROSURGICAL EAR PICKS is JYT.

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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: JYT)

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.

K841355RIGHT ANGLED PICKTreace Medical, 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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