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FDA 510(k)

TRU-PULSE PADS

K-Number: K800117 · 1980-02-11

ApplicantIpco Corp.
Decision Date1980-02-11
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TRU-PULSE PADS is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1980-02-11 under 510(k) number K800117. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRU-PULSE PADS?

TRU-PULSE PADS is a medical device that received FDA 510(k) clearance on 1980-02-11. The listed applicant is Ipco Corp.. The 510(k) number is K800117.

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

TRU-PULSE PADS received FDA 510(k) clearance on 1980-02-11, under 510(k) number K800117.

Who is the listed applicant for TRU-PULSE PADS?

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

What is the FDA product code for TRU-PULSE PADS?

The FDA product code for TRU-PULSE PADS is GXY.

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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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