ELECTROSURGICAL GROUND PAD-DISPERSIVE
K-Number: K830613 · 1983-04-12
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Device Summary
Frequently Asked Questions
What is the ELECTROSURGICAL GROUND PAD-DISPERSIVE?
ELECTROSURGICAL GROUND PAD-DISPERSIVE is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Con Med Equipment, Inc.. The 510(k) number is K830613.
When did ELECTROSURGICAL GROUND PAD-DISPERSIVE receive FDA 510(k) clearance?
ELECTROSURGICAL GROUND PAD-DISPERSIVE received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830613.
Who is the listed applicant for ELECTROSURGICAL GROUND PAD-DISPERSIVE?
The FDA 510(k) record lists Con Med Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTROSURGICAL GROUND PAD-DISPERSIVE?
The FDA product code for ELECTROSURGICAL GROUND PAD-DISPERSIVE 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 Con Med Equipment, 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.
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