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FDA 510(k)

IV BAND (INTRAVENOUS CATHETER ASSESORY)

K-Number: K860706 · 1986-03-21

ApplicantT. G. & E. Medical
Decision Date1986-03-21
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV BAND (INTRAVENOUS CATHETER ASSESORY) is the device name listed in this FDA 510(k) record. The listed applicant is T. G. & E. Medical. It received FDA 510(k) clearance on 1986-03-21 under 510(k) number K860706. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IV BAND (INTRAVENOUS CATHETER ASSESORY)?

IV BAND (INTRAVENOUS CATHETER ASSESORY) is a medical device that received FDA 510(k) clearance on 1986-03-21. The listed applicant is T. G. & E. Medical. The 510(k) number is K860706.

When did IV BAND (INTRAVENOUS CATHETER ASSESORY) receive FDA 510(k) clearance?

IV BAND (INTRAVENOUS CATHETER ASSESORY) received FDA 510(k) clearance on 1986-03-21, under 510(k) number K860706.

Who is the listed applicant for IV BAND (INTRAVENOUS CATHETER ASSESORY)?

The FDA 510(k) record lists T. G. & E. Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IV BAND (INTRAVENOUS CATHETER ASSESORY)?

The FDA product code for IV BAND (INTRAVENOUS CATHETER ASSESORY) is KMK.

Related Clinical Trials

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Other records listing T. G. & E. Medical 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.

K860261CANNULA BANDK823221ACCA-TEMP SKIN TEMP. VINYL DISCK820941THERMA-SCANK813199SKIN TEMPERATURE SENSING VINYL STRIP

Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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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