ELECTROSURGICAL ELECTRODE
K-Number: K925478 · 1994-06-27
Advertisement
Device Summary
Frequently Asked Questions
What is the ELECTROSURGICAL ELECTRODE?
ELECTROSURGICAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K925478.
When did ELECTROSURGICAL ELECTRODE receive FDA 510(k) clearance?
ELECTROSURGICAL ELECTRODE received FDA 510(k) clearance on 1994-06-27, under 510(k) number K925478.
Who is the listed applicant for ELECTROSURGICAL ELECTRODE?
The FDA 510(k) record lists Megadyne Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTROSURGICAL ELECTRODE?
The FDA product code for ELECTROSURGICAL ELECTRODE is HGI.
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 Megadyne Medical Products, 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: HGI)
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