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FDA 510(k)

THEIR ELECTRO SURGICAL COUTERY PENCIL

K-Number: K820156 · 1982-02-18

ApplicantShannon Group
Decision Date1982-02-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THEIR ELECTRO SURGICAL COUTERY PENCIL is the device name listed in this FDA 510(k) record. The listed applicant is Shannon Group. It received FDA 510(k) clearance on 1982-02-18 under 510(k) number K820156. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THEIR ELECTRO SURGICAL COUTERY PENCIL?

THEIR ELECTRO SURGICAL COUTERY PENCIL is a medical device that received FDA 510(k) clearance on 1982-02-18. The listed applicant is Shannon Group. The 510(k) number is K820156.

When did THEIR ELECTRO SURGICAL COUTERY PENCIL receive FDA 510(k) clearance?

THEIR ELECTRO SURGICAL COUTERY PENCIL received FDA 510(k) clearance on 1982-02-18, under 510(k) number K820156.

Who is the listed applicant for THEIR ELECTRO SURGICAL COUTERY PENCIL?

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

What is the FDA product code for THEIR ELECTRO SURGICAL COUTERY PENCIL?

The FDA product code for THEIR ELECTRO SURGICAL COUTERY PENCIL is GEI.

Related Clinical Trials

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Other records listing Shannon Group 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.

K811205MOLDED POLYSULFONE TRIAL PROSTHESIS

Related Devices (Code: GEI)

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Official Source

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