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FDA 510(k)

MALLEUS NIPPERS

K-Number: K822198 · 1982-08-25

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

Device Summary

MALLEUS NIPPERS 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 K822198. The device is classified under product code JEK. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MALLEUS NIPPERS?

MALLEUS NIPPERS 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 K822198.

When did MALLEUS NIPPERS receive FDA 510(k) clearance?

MALLEUS NIPPERS received FDA 510(k) clearance on 1982-08-25, under 510(k) number K822198.

Who is the listed applicant for MALLEUS NIPPERS?

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 MALLEUS NIPPERS?

The FDA product code for MALLEUS NIPPERS is JEK.

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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: JEK)

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.

K990561OPTICAL FORCEPSPilling Weck SurgicalK822193FORCEPS FOR USE WITH RIGID ENDOSCOPESKelleher Corp.

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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