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FDA 510(k)

INCUS NIPPERS

K-Number: K822170 · 1982-08-24

Decision Date1982-08-24
Product CodeJYR
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

INCUS 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 1982-08-24 under 510(k) number K822170. The device is classified under product code JYR. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INCUS NIPPERS?

INCUS NIPPERS is a medical device that received FDA 510(k) clearance on 1982-08-24. The listed applicant is Kelleher Corp.. The 510(k) number is K822170.

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

INCUS NIPPERS received FDA 510(k) clearance on 1982-08-24, under 510(k) number K822170.

Who is the listed applicant for INCUS 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 INCUS NIPPERS?

The FDA product code for INCUS NIPPERS is JYR.

Related Clinical Trials

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.

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.

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Related Devices (Code: JYR)

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.

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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