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FDA 510(k)

DOUBLE-COAGULATION SWITCHPEN 757

K-Number: K834410 · 1984-04-04

Decision Date1984-04-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DOUBLE-COAGULATION SWITCHPEN 757 is the device name listed in this FDA 510(k) record. The listed applicant is Olsen Electro-Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1984-04-04 under 510(k) number K834410. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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