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FDA 510(k)

NON-STERILE PREGELLED GROUNDING PAD

K-Number: K761221 · 1977-01-12

ApplicantIpco Corp.
Decision Date1977-01-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NON-STERILE PREGELLED GROUNDING PAD is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K761221. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-STERILE PREGELLED GROUNDING PAD?

NON-STERILE PREGELLED GROUNDING PAD is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Ipco Corp.. The 510(k) number is K761221.

When did NON-STERILE PREGELLED GROUNDING PAD receive FDA 510(k) clearance?

NON-STERILE PREGELLED GROUNDING PAD received FDA 510(k) clearance on 1977-01-12, under 510(k) number K761221.

Who is the listed applicant for NON-STERILE PREGELLED GROUNDING PAD?

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 NON-STERILE PREGELLED GROUNDING PAD?

The FDA product code for NON-STERILE PREGELLED GROUNDING PAD is GEI.

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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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