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FDA 510(k)

STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER

K-Number: K955152 · 1996-02-22

ApplicantStoeckert Instrumente
Decision Date1996-02-22
Product CodeDTW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER is the device name listed in this FDA 510(k) record. The listed applicant is Stoeckert Instrumente. It received FDA 510(k) clearance on 1996-02-22 under 510(k) number K955152. 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 S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER?

STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER is a medical device that received FDA 510(k) clearance on 1996-02-22. The listed applicant is Stoeckert Instrumente. The 510(k) number is K955152.

When did STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER receive FDA 510(k) clearance?

STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER received FDA 510(k) clearance on 1996-02-22, under 510(k) number K955152.

Who is the listed applicant for STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER?

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

What is the FDA product code for STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER?

The FDA product code for STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER is DTW.

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Other records listing Stoeckert Instrumente 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.

K002273STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAEK001961STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAEK002118STOCKERT COMPACT SYSTEM VERSION 2.0K992635INTERFACE MODULE IDDDK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSK982014STOCKERT COMPACT SYSTEM

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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.K910599CARDIOPULMONARY BYPASS LEVEL SENSING MONITORJtl Medical Corp.K924354STOCKERT CAPS LOW LEVEL DETECT II/BUBBLE MONITORSorin Biomedica, Fiat, USA, Inc.K915337CAPIOX LEVEL ALARMTerumo Medical Corp.K900910COBE AIR EMBOLI PROTECTION SYSTEM (AEPS)Cobe Laboratories, Inc.

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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