COPPER-TRAP
K-Number: K781696 · 1978-11-03
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Device Summary
Frequently Asked Questions
What is the COPPER-TRAP?
COPPER-TRAP is a medical device that received FDA 510(k) clearance on 1978-11-03. The listed applicant is Olympic Medical Corp.. The 510(k) number is K781696.
When did COPPER-TRAP receive FDA 510(k) clearance?
COPPER-TRAP received FDA 510(k) clearance on 1978-11-03, under 510(k) number K781696.
Who is the listed applicant for COPPER-TRAP?
The FDA 510(k) record lists Olympic Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COPPER-TRAP?
The FDA product code for COPPER-TRAP is CAH.
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 Olympic Medical Corp. 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: CAH)
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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