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FDA 510(k)

NON-ADHER PADS

K-Number: K813421 · 1981-12-18

ApplicantAbco Dealers, Inc.
Decision Date1981-12-18
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON-ADHER PADS is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1981-12-18 under 510(k) number K813421. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-ADHER PADS?

NON-ADHER PADS is a medical device that received FDA 510(k) clearance on 1981-12-18. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K813421.

When did NON-ADHER PADS receive FDA 510(k) clearance?

NON-ADHER PADS received FDA 510(k) clearance on 1981-12-18, under 510(k) number K813421.

Who is the listed applicant for NON-ADHER PADS?

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

What is the FDA product code for NON-ADHER PADS?

The FDA product code for NON-ADHER PADS is KGX.

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Other records listing Abco Dealers, Inc. as applicant

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Related Devices (Code: KGX)

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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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