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FDA 510(k)

INTERFACE MODULE IDDD

K-Number: K992635 · 1999-12-20

ApplicantStoeckert Instrumente
Decision Date1999-12-20
Product CodeKRI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERFACE MODULE IDDD is the device name listed in this FDA 510(k) record. The listed applicant is Stoeckert Instrumente. It received FDA 510(k) clearance on 1999-12-20 under 510(k) number K992635. 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 INTERFACE MODULE IDDD?

INTERFACE MODULE IDDD is a medical device that received FDA 510(k) clearance on 1999-12-20. The listed applicant is Stoeckert Instrumente. The 510(k) number is K992635.

When did INTERFACE MODULE IDDD receive FDA 510(k) clearance?

INTERFACE MODULE IDDD received FDA 510(k) clearance on 1999-12-20, under 510(k) number K992635.

Who is the listed applicant for INTERFACE MODULE IDDD?

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 INTERFACE MODULE IDDD?

The FDA product code for INTERFACE MODULE IDDD is KRI.

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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 2.0K990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSK982014STOCKERT COMPACT SYSTEMK972321S3 MAST PUMP

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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, LLCK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert 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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