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FDA 510(k)

TECNOL SECURE-ALL TUBE HOLDER

K-Number: K891178 · 1989-05-23

ApplicantTecnol New Jersey Wound Care, Inc.
Decision Date1989-05-23
Product CodeEYZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TECNOL SECURE-ALL TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol New Jersey Wound Care, Inc.. It received FDA 510(k) clearance on 1989-05-23 under 510(k) number K891178. The device is classified under product code EYZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECNOL SECURE-ALL TUBE HOLDER?

TECNOL SECURE-ALL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1989-05-23. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K891178.

When did TECNOL SECURE-ALL TUBE HOLDER receive FDA 510(k) clearance?

TECNOL SECURE-ALL TUBE HOLDER received FDA 510(k) clearance on 1989-05-23, under 510(k) number K891178.

Who is the listed applicant for TECNOL SECURE-ALL TUBE HOLDER?

The FDA 510(k) record lists Tecnol New Jersey Wound Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECNOL SECURE-ALL TUBE HOLDER?

The FDA product code for TECNOL SECURE-ALL TUBE HOLDER is EYZ.

Related Clinical Trials

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Other records listing Tecnol New Jersey Wound Care, Inc. 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.

K913043MODIFICATION TECNOL FLUIDSHIELD SURGICAL MASKSK911891FLUIDSHIELD(TM) CONE CLASSIC(TM) II SURGICAL MASKK911907FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VISK896193TECNOL LAZER(TM) SURGICAL MASKK894205TECNOL SILK STRIPK893702TECNOL GAITERS PRODUCT NUMBER 47725-010

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Related Devices (Code: EYZ)

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.

K964219ZIP CONDOM CATHETERGoulter Medical, Inc.K961906UNI-GARD QUIK CATH(SIZES 8 FRENCH THROUGH 18)UG 10008,10010,10012,10014,10016,10018Spectrum Medsystems Corp.K952780URINARY GEL DRAINAGE SYSTEMP.A.M., Inc.K951597URINARY DRAINAGE BAGKey Medical Services, Inc.K942753ONE STEP SPECIMEN COLLECTOR/TRANSPORT CONTAINERResearched, Novel Medical Devices (Rn/Md)K933126COMFORTCARE SYSTEMPatsy J. Trisler, J.D.

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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