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FDA 510(k)

#875 DISPOSABLE BIOPOLAR CABLE

K-Number: K884171 · 1988-10-24

Decision Date1988-10-24
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

#875 DISPOSABLE BIOPOLAR CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Olsen Electrosurgical, Inc.. It received FDA 510(k) clearance on 1988-10-24 under 510(k) number K884171. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the #875 DISPOSABLE BIOPOLAR CABLE?

#875 DISPOSABLE BIOPOLAR CABLE is a medical device that received FDA 510(k) clearance on 1988-10-24. The listed applicant is Olsen Electrosurgical, Inc.. The 510(k) number is K884171.

When did #875 DISPOSABLE BIOPOLAR CABLE receive FDA 510(k) clearance?

#875 DISPOSABLE BIOPOLAR CABLE received FDA 510(k) clearance on 1988-10-24, under 510(k) number K884171.

Who is the listed applicant for #875 DISPOSABLE BIOPOLAR CABLE?

The FDA 510(k) record lists Olsen Electrosurgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for #875 DISPOSABLE BIOPOLAR CABLE?

The FDA product code for #875 DISPOSABLE BIOPOLAR CABLE is HAM.

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 Electrosurgical, 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.

View all 11 devices →

Related Devices (Code: HAM)

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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