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FDA 510(k)

ENT METAL TONGUE DEPRESSORS

K-Number: K822184 · 1982-08-16

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

Device Summary

ENT METAL TONGUE DEPRESSORS 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 K822184. The device is classified under product code KBL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENT METAL TONGUE DEPRESSORS?

ENT METAL TONGUE DEPRESSORS 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 K822184.

When did ENT METAL TONGUE DEPRESSORS receive FDA 510(k) clearance?

ENT METAL TONGUE DEPRESSORS received FDA 510(k) clearance on 1982-08-16, under 510(k) number K822184.

Who is the listed applicant for ENT METAL TONGUE DEPRESSORS?

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 METAL TONGUE DEPRESSORS?

The FDA product code for ENT METAL TONGUE DEPRESSORS is KBL.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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