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FDA 510(k)

ELECTRO-PULSE

K-Number: K832160 · 1983-11-14

ApplicantElectro-Pulse
Decision Date1983-11-14
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-PULSE is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Pulse. It received FDA 510(k) clearance on 1983-11-14 under 510(k) number K832160. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-PULSE?

ELECTRO-PULSE is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Electro-Pulse. The 510(k) number is K832160.

When did ELECTRO-PULSE receive FDA 510(k) clearance?

ELECTRO-PULSE received FDA 510(k) clearance on 1983-11-14, under 510(k) number K832160.

Who is the listed applicant for ELECTRO-PULSE?

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

What is the FDA product code for ELECTRO-PULSE?

The FDA product code for ELECTRO-PULSE is GZJ.

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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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