FDA 510(k)

IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003

K-Number: K912229 · 1991-09-25

Decision Date1991-09-25

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003 is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1991-09-25 under 510(k) number K912229. 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 IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003?

IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003 is a medical device that received FDA 510(k) clearance on 1991-09-25. The listed applicant is Dlp, Inc.. The 510(k) number is K912229.

When did IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003 receive FDA 510(k) clearance?

IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003 received FDA 510(k) clearance on 1991-09-25, under 510(k) number K912229.

Who is the listed applicant for IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003?

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

What is the FDA product code for IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003?

The FDA product code for IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003 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.