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FDA 510(k)

MAYO SCISSOR CURYED 5 1/2

K-Number: K821276 · 1982-05-28

ApplicantConphar, Inc.
Decision Date1982-05-28
Product CodeEGN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MAYO SCISSOR CURYED 5 1/2 is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-05-28 under 510(k) number K821276. The device is classified under product code EGN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAYO SCISSOR CURYED 5 1/2?

MAYO SCISSOR CURYED 5 1/2 is a medical device that received FDA 510(k) clearance on 1982-05-28. The listed applicant is Conphar, Inc.. The 510(k) number is K821276.

When did MAYO SCISSOR CURYED 5 1/2 receive FDA 510(k) clearance?

MAYO SCISSOR CURYED 5 1/2 received FDA 510(k) clearance on 1982-05-28, under 510(k) number K821276.

Who is the listed applicant for MAYO SCISSOR CURYED 5 1/2?

The FDA 510(k) record lists Conphar, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAYO SCISSOR CURYED 5 1/2?

The FDA product code for MAYO SCISSOR CURYED 5 1/2 is EGN.

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 Conphar, Inc. 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 122 devices →

Related Devices (Code: EGN)

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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