CLEAR POROUS PLASTIC-HYPOALLERGENIC
K-Number: K840948 · 1984-08-14
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Device Summary
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.
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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