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FDA 510(k)

AMMEX TUBING ORGANIZER

K-Number: K934782 · 1993-11-18

ApplicantAmmex Cardiopulmonary Corp.
Decision Date1993-11-18
Product CodeKRI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMMEX TUBING ORGANIZER is the device name listed in this FDA 510(k) record. The listed applicant is Ammex Cardiopulmonary Corp.. It received FDA 510(k) clearance on 1993-11-18 under 510(k) number K934782. 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 AMMEX TUBING ORGANIZER?

AMMEX TUBING ORGANIZER is a medical device that received FDA 510(k) clearance on 1993-11-18. The listed applicant is Ammex Cardiopulmonary Corp.. The 510(k) number is K934782.

When did AMMEX TUBING ORGANIZER receive FDA 510(k) clearance?

AMMEX TUBING ORGANIZER received FDA 510(k) clearance on 1993-11-18, under 510(k) number K934782.

Who is the listed applicant for AMMEX TUBING ORGANIZER?

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

What is the FDA product code for AMMEX TUBING ORGANIZER?

The FDA product code for AMMEX TUBING ORGANIZER is KRI.

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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, LLCK992635INTERFACE MODULE IDDDStoeckert InstrumenteK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert InstrumenteK926233CARDIO2 CYCLEErgometrix, Inc.K922404TUBE GRIPGeorgia Medical Products, Inc.K892856NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERSAcacia Laboratories, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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