FDA 510(k)

TUBE GRIP

K-Number: K922404 · 1992-11-23

Decision Date1992-11-23

Product CodeKRI

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

TUBE GRIP is the device name listed in this FDA 510(k) record. The listed applicant is Georgia Medical Products, Inc.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K922404. 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 TUBE GRIP?

TUBE GRIP is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Georgia Medical Products, Inc.. The 510(k) number is K922404.

When did TUBE GRIP receive FDA 510(k) clearance?

TUBE GRIP received FDA 510(k) clearance on 1992-11-23, under 510(k) number K922404.

Who is the listed applicant for TUBE GRIP?

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

What is the FDA product code for TUBE GRIP?

The FDA product code for TUBE GRIP is KRI.

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, LLC K992635INTERFACE MODULE IDDDStoeckert Instrumente K990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert Instrumente K934782AMMEX TUBING ORGANIZERAmmex Cardiopulmonary Corp.K926233CARDIO2 CYCLEErgometrix, 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.