MODEL 200C ELECTROSURGICAL PROBE
K-Number: K960695 · 1996-04-30
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Device Summary
Frequently Asked Questions
What is the MODEL 200C ELECTROSURGICAL PROBE?
MODEL 200C ELECTROSURGICAL PROBE is a medical device that received FDA 510(k) clearance on 1996-04-30. The listed applicant is Zomed Intl.. The 510(k) number is K960695.
When did MODEL 200C ELECTROSURGICAL PROBE receive FDA 510(k) clearance?
MODEL 200C ELECTROSURGICAL PROBE received FDA 510(k) clearance on 1996-04-30, under 510(k) number K960695.
Who is the listed applicant for MODEL 200C ELECTROSURGICAL PROBE?
The FDA 510(k) record lists Zomed Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 200C ELECTROSURGICAL PROBE?
The FDA product code for MODEL 200C ELECTROSURGICAL PROBE 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 Zomed Intl. 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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