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FDA 510(k)

DISP. METAL & PLASTIC ELECTROSURG. DEV

K-Number: K822355 · 1982-09-22

ApplicantValleylab, Inc.
Decision Date1982-09-22
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISP. METAL & PLASTIC ELECTROSURG. DEV is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1982-09-22 under 510(k) number K822355. 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 DISP. METAL & PLASTIC ELECTROSURG. DEV?

DISP. METAL & PLASTIC ELECTROSURG. DEV is a medical device that received FDA 510(k) clearance on 1982-09-22. The listed applicant is Valleylab, Inc.. The 510(k) number is K822355.

When did DISP. METAL & PLASTIC ELECTROSURG. DEV receive FDA 510(k) clearance?

DISP. METAL & PLASTIC ELECTROSURG. DEV received FDA 510(k) clearance on 1982-09-22, under 510(k) number K822355.

Who is the listed applicant for DISP. METAL & PLASTIC ELECTROSURG. DEV?

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

What is the FDA product code for DISP. METAL & PLASTIC ELECTROSURG. DEV?

The FDA product code for DISP. METAL & PLASTIC ELECTROSURG. DEV is GEI.

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Related Devices (Code: GEI)

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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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