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FDA 510(k)

ANALGESIC PULSER, MODEL AP-439

K-Number: K993229 · 2001-02-02

ApplicantJohari Electro-Tech Co.
Decision Date2001-02-02
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ANALGESIC PULSER, MODEL AP-439 is the device name listed in this FDA 510(k) record. The listed applicant is Johari Electro-Tech Co.. It received FDA 510(k) clearance on 2001-02-02 under 510(k) number K993229. 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 ANALGESIC PULSER, MODEL AP-439?

ANALGESIC PULSER, MODEL AP-439 is a medical device that received FDA 510(k) clearance on 2001-02-02. The listed applicant is Johari Electro-Tech Co.. The 510(k) number is K993229.

When did ANALGESIC PULSER, MODEL AP-439 receive FDA 510(k) clearance?

ANALGESIC PULSER, MODEL AP-439 received FDA 510(k) clearance on 2001-02-02, under 510(k) number K993229.

Who is the listed applicant for ANALGESIC PULSER, MODEL AP-439?

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

What is the FDA product code for ANALGESIC PULSER, MODEL AP-439?

The FDA product code for ANALGESIC PULSER, MODEL AP-439 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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