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FDA 510(k)

MIRCOSURGICAL INSTRUMENTS

K-Number: K822195 · 1982-08-25

Decision Date1982-08-25
Product CodeJYL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MIRCOSURGICAL INSTRUMENTS 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 K822195. The device is classified under product code JYL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIRCOSURGICAL INSTRUMENTS?

MIRCOSURGICAL INSTRUMENTS 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 K822195.

When did MIRCOSURGICAL INSTRUMENTS receive FDA 510(k) clearance?

MIRCOSURGICAL INSTRUMENTS received FDA 510(k) clearance on 1982-08-25, under 510(k) number K822195.

Who is the listed applicant for MIRCOSURGICAL INSTRUMENTS?

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 MIRCOSURGICAL INSTRUMENTS?

The FDA product code for MIRCOSURGICAL INSTRUMENTS is JYL.

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.

View all 94 devices →

Related Devices (Code: JYL)

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

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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