ARTERIAL BUBBLE TRAP
K-Number: K801770 · 1980-08-07
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Device Summary
Frequently Asked Questions
What is the ARTERIAL BUBBLE TRAP?
ARTERIAL BUBBLE TRAP is a medical device that received FDA 510(k) clearance on 1980-08-07. The listed applicant is Delta Medical Industries. The 510(k) number is K801770.
When did ARTERIAL BUBBLE TRAP receive FDA 510(k) clearance?
ARTERIAL BUBBLE TRAP received FDA 510(k) clearance on 1980-08-07, under 510(k) number K801770.
Who is the listed applicant for ARTERIAL BUBBLE TRAP?
The FDA 510(k) record lists Delta Medical Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTERIAL BUBBLE TRAP?
The FDA product code for ARTERIAL BUBBLE TRAP is DWF.
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 Delta Medical Industries 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: DWF)
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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