MIDAS TOUCH ELECTROSURGICAL ELECTRODE
K-Number: K973234 · 1997-10-27
Advertisement
Device Summary
Frequently Asked Questions
What is the MIDAS TOUCH ELECTROSURGICAL ELECTRODE?
MIDAS TOUCH ELECTROSURGICAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1997-10-27. The listed applicant is Iti Medical Technologies, Inc.. The 510(k) number is K973234.
When did MIDAS TOUCH ELECTROSURGICAL ELECTRODE receive FDA 510(k) clearance?
MIDAS TOUCH ELECTROSURGICAL ELECTRODE received FDA 510(k) clearance on 1997-10-27, under 510(k) number K973234.
Who is the listed applicant for MIDAS TOUCH ELECTROSURGICAL ELECTRODE?
The FDA 510(k) record lists Iti Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIDAS TOUCH ELECTROSURGICAL ELECTRODE?
The FDA product code for MIDAS TOUCH ELECTROSURGICAL ELECTRODE is GEI.
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 Iti Medical Technologies, 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.
Related Devices (Code: GEI)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement