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FDA 510(k)

SARNS INFANT ARTERIAL BUBBLE SENSOR

K-Number: K803105 · 1980-12-31

Decision Date1980-12-31
Product CodeKPL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SARNS INFANT ARTERIAL BUBBLE SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Sarns. It received FDA 510(k) clearance on 1980-12-31 under 510(k) number K803105. The device is classified under product code KPL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARNS INFANT ARTERIAL BUBBLE SENSOR?

SARNS INFANT ARTERIAL BUBBLE SENSOR is a medical device that received FDA 510(k) clearance on 1980-12-31. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K803105.

When did SARNS INFANT ARTERIAL BUBBLE SENSOR receive FDA 510(k) clearance?

SARNS INFANT ARTERIAL BUBBLE SENSOR received FDA 510(k) clearance on 1980-12-31, under 510(k) number K803105.

Who is the listed applicant for SARNS INFANT ARTERIAL BUBBLE SENSOR?

The FDA 510(k) record lists 3M Health Care, Sarns as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SARNS INFANT ARTERIAL BUBBLE SENSOR?

The FDA product code for SARNS INFANT ARTERIAL BUBBLE SENSOR is KPL.

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 3M Health Care, Sarns 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 76 devices →

Related Devices (Code: KPL)

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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