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FDA 510(k)

PULSATOR 5000

K-Number: K930102 · 1994-03-23

ApplicantToys House Industrial Corp.
Decision Date1994-03-23
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PULSATOR 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Toys House Industrial Corp.. It received FDA 510(k) clearance on 1994-03-23 under 510(k) number K930102. 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 PULSATOR 5000?

PULSATOR 5000 is a medical device that received FDA 510(k) clearance on 1994-03-23. The listed applicant is Toys House Industrial Corp.. The 510(k) number is K930102.

When did PULSATOR 5000 receive FDA 510(k) clearance?

PULSATOR 5000 received FDA 510(k) clearance on 1994-03-23, under 510(k) number K930102.

Who is the listed applicant for PULSATOR 5000?

The FDA 510(k) record lists Toys House Industrial Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PULSATOR 5000?

The FDA product code for PULSATOR 5000 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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