ARTERIAL BUBBLE TRAP K-20
K-Number: K803102 · 1980-12-22
Device Summary
Frequently Asked Questions
What is the ARTERIAL BUBBLE TRAP K-20?
ARTERIAL BUBBLE TRAP K-20 is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Delta Medical Industries. The 510(k) number is K803102.
When did ARTERIAL BUBBLE TRAP K-20 receive FDA 510(k) clearance?
ARTERIAL BUBBLE TRAP K-20 received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803102.
Who is the listed applicant for ARTERIAL BUBBLE TRAP K-20?
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 K-20?
The FDA product code for ARTERIAL BUBBLE TRAP K-20 is KRL.
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: KRL)
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.