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FDA 510(k)

NEURO PULSE

K-Number: K841400 · 1984-06-15

ApplicantParker Laboratories, Inc.
Decision Date1984-06-15
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURO PULSE is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1984-06-15 under 510(k) number K841400. 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 NEURO PULSE?

NEURO PULSE is a medical device that received FDA 510(k) clearance on 1984-06-15. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K841400.

When did NEURO PULSE receive FDA 510(k) clearance?

NEURO PULSE received FDA 510(k) clearance on 1984-06-15, under 510(k) number K841400.

Who is the listed applicant for NEURO PULSE?

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

What is the FDA product code for NEURO PULSE?

The FDA product code for NEURO PULSE is GZJ.

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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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