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FDA 510(k)

AIR BUBBLE DETECTOR

K-Number: K781021 · 1978-09-27

Applicant3M Health Care, Sarns
Decision Date1978-09-27
Product Code
DecisionSubstantially Equivalent

Device Summary

AIR BUBBLE DETECTOR 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 1978-09-27 under 510(k) number K781021. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR BUBBLE DETECTOR?

AIR BUBBLE DETECTOR is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K781021.

When did AIR BUBBLE DETECTOR receive FDA 510(k) clearance?

AIR BUBBLE DETECTOR received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781021.

Who is the listed applicant for AIR BUBBLE DETECTOR?

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

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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.

K960916SAMS 8000 CARDIOPLEGIA MONITORK953901SARNS 800 ROLLER PUMPK9507393M SARNS FLOW SENSOR, CENTRIFUGAL CONTROL MODULE 115, 220 V, 900 PERFUSION SYSTEMK941653SARNS TURBO MEMBRANE OXYGENATOR MODIFICATIONK941654SARNS FILTERED VENOUS RESERVIOR MODIFICATIONK940651SARNS ULTRASONIC AIR SENSOR

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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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