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FDA 510(k)

STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE

K-Number: K061660 · 2006-10-10

Decision Date2006-10-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2006-10-10 under 510(k) number K061660. 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 STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE?

STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE is a medical device that received FDA 510(k) clearance on 2006-10-10. The listed applicant is Stryker Instruments. The 510(k) number is K061660.

When did STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE receive FDA 510(k) clearance?

STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE received FDA 510(k) clearance on 2006-10-10, under 510(k) number K061660.

Who is the listed applicant for STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE?

The FDA 510(k) record lists Stryker Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE?

The FDA product code for STRYKER RF PARALLEL BIPOLAR ADAPTOR CABLE 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 Stryker Instruments 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 75 devices →

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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