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FDA 510(k)

KIT PAK WET SALINE DRESSING

K-Number: K942959 · 1995-02-14

ApplicantKit Pak, Inc.
Decision Date1995-02-14
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

KIT PAK WET SALINE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Kit Pak, Inc.. It received FDA 510(k) clearance on 1995-02-14 under 510(k) number K942959. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the KIT PAK WET SALINE DRESSING?

KIT PAK WET SALINE DRESSING is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is Kit Pak, Inc.. The 510(k) number is K942959.

When did KIT PAK WET SALINE DRESSING receive FDA 510(k) clearance?

KIT PAK WET SALINE DRESSING received FDA 510(k) clearance on 1995-02-14, under 510(k) number K942959.

Who is the listed applicant for KIT PAK WET SALINE DRESSING?

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

What is the FDA product code for KIT PAK WET SALINE DRESSING?

The FDA product code for KIT PAK WET SALINE DRESSING is FRO. This falls under the Anesthesiology category.

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Other records listing Kit Pak, 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.

K941499KIT PAK DRESSING CHANGE TRAYK932310KIT PAK INCONTINENT SKIN CARE KITK934080URINARY DRAINAGE BAGK931013FOLEY CATHETER TRAYK923905WOUND DRESSING KITK924051KIT PAK I.V. START KIT

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Related Devices (Code: FRO)

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.

K254168Actolind® (06.3637. Actolind® Gel Plus)ACTO GmbHK254041SkinSmart Antimicrobial HydroGelMagic Science Supply, LLCK261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.K253665Vashe Plus Antimicrobial SolutionUrgo Medical North America, LLCK251929SilverCeuticals® Antimicrobial Wound GelSilverceuticals, Inc.K261023Microdacyn Wound Irrigation SolutionSonoma Pharmaceuticals, 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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