FDA 510(k)

E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS

K-Number: K945260 · 1994-11-09

Decision Date1994-11-09

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1994-11-09 under 510(k) number K945260. 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 E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS?

E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS is a medical device that received FDA 510(k) clearance on 1994-11-09. The listed applicant is Valleylab, Inc.. The 510(k) number is K945260.

When did E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS receive FDA 510(k) clearance?

E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS received FDA 510(k) clearance on 1994-11-09, under 510(k) number K945260.

Who is the listed applicant for E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS?

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 E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS?

The FDA product code for E3590, SMOKE EVACUATION ATTCHMENT FOR ELECTROSURGICAL PENCILS is GEI.

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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.