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FDA 510(k)

VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE

K-Number: K895993 · 1990-01-11

ApplicantVitaphore Corp.
Decision Date1990-01-11
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Vitaphore Corp.. It received FDA 510(k) clearance on 1990-01-11 under 510(k) number K895993. 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 VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE?

VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE is a medical device that received FDA 510(k) clearance on 1990-01-11. The listed applicant is Vitaphore Corp.. The 510(k) number is K895993.

When did VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE receive FDA 510(k) clearance?

VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE received FDA 510(k) clearance on 1990-01-11, under 510(k) number K895993.

Who is the listed applicant for VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE?

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

What is the FDA product code for VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE?

The FDA product code for VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE is KMK.

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Other records listing Vitaphore Corp. 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.

K914579SILVER FOAM WOUND DRESSINGK913148COLLAGEN SHIELD FOR ACUTE CAREK895920VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUSK902558COLLAGEN SHIELD FOR ACUTE CAREK891993COLLAGEN NEUROSPONGEK896455VITACHOICE WOUND DRESSING

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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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