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FDA 510(k)

VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS

K-Number: K895920 · 1991-06-06

ApplicantVitaphore Corp.
Decision Date1991-06-06
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS is the device name listed in this FDA 510(k) record. The listed applicant is Vitaphore Corp.. It received FDA 510(k) clearance on 1991-06-06 under 510(k) number K895920. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS?

VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is Vitaphore Corp.. The 510(k) number is K895920.

When did VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS receive FDA 510(k) clearance?

VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS received FDA 510(k) clearance on 1991-06-06, under 510(k) number K895920.

Who is the listed applicant for VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS?

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 PIN PROTECTION DEVICE FOR PERCUTANEOUS?

The FDA product code for VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS is KGX.

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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 CAREK902558COLLAGEN SHIELD FOR ACUTE CAREK891993COLLAGEN NEUROSPONGEK896455VITACHOICE WOUND DRESSINGK895993VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE

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Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, 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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