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FDA 510(k)

ARTERIAL BUBBLE TRAP K-20

K-Number: K803102 · 1980-12-22

Decision Date1980-12-22
Product CodeKRL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARTERIAL BUBBLE TRAP K-20 is the device name listed in this FDA 510(k) record. The listed applicant is Delta Medical Industries. It received FDA 510(k) clearance on 1980-12-22 under 510(k) number K803102. The device is classified under product code KRL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 27 devices →

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.

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