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FDA 510(k)

SPARTA WET DRESSING, SODIUM CHLORIDE

K-Number: K922729 · 1992-11-23

ApplicantSparta Surgical Corp.
Decision Date1992-11-23
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

SPARTA WET DRESSING, SODIUM CHLORIDE is the device name listed in this FDA 510(k) record. The listed applicant is Sparta Surgical Corp.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K922729. 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 SPARTA WET DRESSING, SODIUM CHLORIDE?

SPARTA WET DRESSING, SODIUM CHLORIDE is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Sparta Surgical Corp.. The 510(k) number is K922729.

When did SPARTA WET DRESSING, SODIUM CHLORIDE receive FDA 510(k) clearance?

SPARTA WET DRESSING, SODIUM CHLORIDE received FDA 510(k) clearance on 1992-11-23, under 510(k) number K922729.

Who is the listed applicant for SPARTA WET DRESSING, SODIUM CHLORIDE?

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

What is the FDA product code for SPARTA WET DRESSING, SODIUM CHLORIDE?

The FDA product code for SPARTA WET DRESSING, SODIUM CHLORIDE is FRO. This falls under the Anesthesiology category.

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Other records listing Sparta Surgical 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.

K965187SPECTRUM II, SPECTRUM PLUS, AND SPECTRUM MAX-SDK945313SPARTA HYDROGEL WOUND DRESSINGK905384DAVID SIMMONDS ANESTHESIA EXTENSION TUBESK905240VESSELOOPSK896085SURGI-BRUSHK896084MICROSPEARS

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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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