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FDA 510(k)

CLEAR POROUS PLASTIC-HYPOALLERGENIC

K-Number: K840948 · 1984-08-14

Decision Date1984-08-14
Product CodeGKX
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CLEAR POROUS PLASTIC-HYPOALLERGENIC is the device name listed in this FDA 510(k) record. The listed applicant is Gainor Medical. It received FDA 510(k) clearance on 1984-08-14 under 510(k) number K840948. The device is classified under product code GKX. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAR POROUS PLASTIC-HYPOALLERGENIC?

CLEAR POROUS PLASTIC-HYPOALLERGENIC is a medical device that received FDA 510(k) clearance on 1984-08-14. The listed applicant is Gainor Medical. The 510(k) number is K840948.

When did CLEAR POROUS PLASTIC-HYPOALLERGENIC receive FDA 510(k) clearance?

CLEAR POROUS PLASTIC-HYPOALLERGENIC received FDA 510(k) clearance on 1984-08-14, under 510(k) number K840948.

Who is the listed applicant for CLEAR POROUS PLASTIC-HYPOALLERGENIC?

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

What is the FDA product code for CLEAR POROUS PLASTIC-HYPOALLERGENIC?

The FDA product code for CLEAR POROUS PLASTIC-HYPOALLERGENIC is GKX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Gainor Medical as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 11 devices →

Related Devices (Code: GKX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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