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FDA 510(k)

STOCKERT-SHILEY UNIVERSAL LEVEL SENSOR

K-Number: K843802 · 1984-12-27

ApplicantShiley, Inc.
Decision Date1984-12-27
Product CodeDTW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT-SHILEY UNIVERSAL LEVEL SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1984-12-27 under 510(k) number K843802. 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 STOCKERT-SHILEY UNIVERSAL LEVEL SENSOR?

STOCKERT-SHILEY UNIVERSAL LEVEL SENSOR is a medical device that received FDA 510(k) clearance on 1984-12-27. The listed applicant is Shiley, Inc.. The 510(k) number is K843802.

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

STOCKERT-SHILEY UNIVERSAL LEVEL SENSOR received FDA 510(k) clearance on 1984-12-27, under 510(k) number K843802.

Who is the listed applicant for STOCKERT-SHILEY UNIVERSAL LEVEL SENSOR?

The FDA 510(k) record lists Shiley, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STOCKERT-SHILEY UNIVERSAL LEVEL SENSOR?

The FDA product code for STOCKERT-SHILEY UNIVERSAL LEVEL SENSOR is DTW.

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Other records listing Shiley, Inc. 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.

K920594SHILEY PERFUSION TUBING SETSK910991SHILEY THERAPEUTIC AUTOTRANSFUSION SYSTEMK911876SHILEY PLEXUS(R) VENOUS RESERVOIR, PVR1200K910923BCD ADVANCEDK901548BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GASK903435SHILEY SPECIALIZED TRACHEOSTOMY TUBE

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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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