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FDA 510(k)

UNIVERSAL LEVEL SENSOR

K-Number: K831879 · 1983-07-26

Applicant3M Health Care, Sarns
Decision Date1983-07-26
Product CodeDTW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL LEVEL 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 1983-07-26 under 510(k) number K831879. The device is classified under product code DTW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL LEVEL SENSOR?

UNIVERSAL LEVEL SENSOR is a medical device that received FDA 510(k) clearance on 1983-07-26. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K831879.

When did UNIVERSAL LEVEL SENSOR receive FDA 510(k) clearance?

UNIVERSAL LEVEL SENSOR received FDA 510(k) clearance on 1983-07-26, under 510(k) number K831879.

Who is the listed applicant for UNIVERSAL LEVEL 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 UNIVERSAL LEVEL SENSOR?

The FDA product code for UNIVERSAL LEVEL SENSOR is DTW.

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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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Related Devices (Code: DTW)

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.

K041558STOCKERTIR PURGE CONTROL (APC) SYSTEMStockert Instrumente GmbHK992857LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070Rocky Mountain Research, Inc.K955152STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMERStoeckert InstrumenteK910599CARDIOPULMONARY BYPASS LEVEL SENSING MONITORJtl Medical Corp.K924354STOCKERT CAPS LOW LEVEL DETECT II/BUBBLE MONITORSorin Biomedica, Fiat, USA, Inc.K915337CAPIOX LEVEL ALARMTerumo Medical Corp.

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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