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FDA 510(k)

B & L ELECTRODE

K-Number: K952655 · 1995-09-28

ApplicantB & L Engineering
Decision Date1995-09-28
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

B & L ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is B & L Engineering. It received FDA 510(k) clearance on 1995-09-28 under 510(k) number K952655. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B & L ELECTRODE?

B & L ELECTRODE is a medical device that received FDA 510(k) clearance on 1995-09-28. The listed applicant is B & L Engineering. The 510(k) number is K952655.

When did B & L ELECTRODE receive FDA 510(k) clearance?

B & L ELECTRODE received FDA 510(k) clearance on 1995-09-28, under 510(k) number K952655.

Who is the listed applicant for B & L ELECTRODE?

The FDA 510(k) record lists B & L Engineering as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for B & L ELECTRODE?

The FDA product code for B & L ELECTRODE is IKN.

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Related Devices (Code: IKN)

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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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