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FDA 510(k)

STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS

K-Number: K990512 · 1999-11-23

ApplicantStoeckert Instrumente
Decision Date1999-11-23
Product CodeKRI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS is the device name listed in this FDA 510(k) record. The listed applicant is Stoeckert Instrumente. It received FDA 510(k) clearance on 1999-11-23 under 510(k) number K990512. The device is classified under product code KRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS?

STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS is a medical device that received FDA 510(k) clearance on 1999-11-23. The listed applicant is Stoeckert Instrumente. The 510(k) number is K990512.

When did STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS receive FDA 510(k) clearance?

STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS received FDA 510(k) clearance on 1999-11-23, under 510(k) number K990512.

Who is the listed applicant for STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS?

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 POWER SUPPLY UNIT FOR S3 COMPONENTS?

The FDA product code for STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS is KRI.

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.

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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 IDDDK982014STOCKERT COMPACT SYSTEMK972321S3 MAST PUMP

View all 13 devices →

Related Devices (Code: KRI)

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.

K0203653TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE3t Medical Systems, LLCK992635INTERFACE MODULE IDDDStoeckert InstrumenteK934782AMMEX TUBING ORGANIZERAmmex Cardiopulmonary Corp.K926233CARDIO2 CYCLEErgometrix, Inc.K922404TUBE GRIPGeorgia Medical Products, Inc.K892856NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERSAcacia 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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