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FDA 510(k)

THE ORIGINAL PULSE-PAK

K-Number: K892639 · 1989-10-05

ApplicantJones Sales Co.
Decision Date1989-10-05
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE ORIGINAL PULSE-PAK is the device name listed in this FDA 510(k) record. The listed applicant is Jones Sales Co.. It received FDA 510(k) clearance on 1989-10-05 under 510(k) number K892639. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ORIGINAL PULSE-PAK?

THE ORIGINAL PULSE-PAK is a medical device that received FDA 510(k) clearance on 1989-10-05. The listed applicant is Jones Sales Co.. The 510(k) number is K892639.

When did THE ORIGINAL PULSE-PAK receive FDA 510(k) clearance?

THE ORIGINAL PULSE-PAK received FDA 510(k) clearance on 1989-10-05, under 510(k) number K892639.

Who is the listed applicant for THE ORIGINAL PULSE-PAK?

The FDA 510(k) record lists Jones Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE ORIGINAL PULSE-PAK?

The FDA product code for THE ORIGINAL PULSE-PAK is NFB.

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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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