DOUBLE-COAGULATION SWITCHPEN 757
K-Number: K834410 · 1984-04-04
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Device Summary
Frequently Asked Questions
What is the DOUBLE-COAGULATION SWITCHPEN 757?
DOUBLE-COAGULATION SWITCHPEN 757 is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Olsen Electro-Surgical Instruments, Inc.. The 510(k) number is K834410.
When did DOUBLE-COAGULATION SWITCHPEN 757 receive FDA 510(k) clearance?
DOUBLE-COAGULATION SWITCHPEN 757 received FDA 510(k) clearance on 1984-04-04, under 510(k) number K834410.
Who is the listed applicant for DOUBLE-COAGULATION SWITCHPEN 757?
The FDA 510(k) record lists Olsen Electro-Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOUBLE-COAGULATION SWITCHPEN 757?
The FDA product code for DOUBLE-COAGULATION SWITCHPEN 757 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 Olsen Electro-Surgical Instruments, 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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