BASIN, LARGE OR SMALL
K-Number: K760492 · 1976-11-12
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Device Summary
Frequently Asked Questions
What is the BASIN, LARGE OR SMALL?
BASIN, LARGE OR SMALL is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Landmark Plastics. The 510(k) number is K760492.
When did BASIN, LARGE OR SMALL receive FDA 510(k) clearance?
BASIN, LARGE OR SMALL received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760492.
Who is the listed applicant for BASIN, LARGE OR SMALL?
The FDA 510(k) record lists Landmark Plastics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BASIN, LARGE OR SMALL?
The FDA product code for BASIN, LARGE OR SMALL is FNY.
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 Landmark Plastics 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: FNY)
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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