REPROCESSED ELECTROSURGICAL ELECTRODES
K-Number: K012669 · 2002-06-27
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Device Summary
Frequently Asked Questions
What is the REPROCESSED ELECTROSURGICAL ELECTRODES?
REPROCESSED ELECTROSURGICAL ELECTRODES is a medical device that received FDA 510(k) clearance on 2002-06-27. The listed applicant is Surgical Instruments Service and Savings, Inc.. The 510(k) number is K012669.
When did REPROCESSED ELECTROSURGICAL ELECTRODES receive FDA 510(k) clearance?
REPROCESSED ELECTROSURGICAL ELECTRODES received FDA 510(k) clearance on 2002-06-27, under 510(k) number K012669.
Who is the listed applicant for REPROCESSED ELECTROSURGICAL ELECTRODES?
The FDA 510(k) record lists Surgical Instruments Service and Savings, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REPROCESSED ELECTROSURGICAL ELECTRODES?
The FDA product code for REPROCESSED ELECTROSURGICAL ELECTRODES 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 Surgical Instruments Service and Savings, 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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