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FDA 510(k)

SPARTA HYDROGEL WOUND DRESSING

K-Number: K945313 · 1995-01-12

ApplicantSparta Surgical Corp.
Decision Date1995-01-12
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

SPARTA HYDROGEL WOUND DRESSING 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 1995-01-12 under 510(k) number K945313. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPARTA HYDROGEL WOUND DRESSING?

SPARTA HYDROGEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-01-12. The listed applicant is Sparta Surgical Corp.. The 510(k) number is K945313.

When did SPARTA HYDROGEL WOUND DRESSING receive FDA 510(k) clearance?

SPARTA HYDROGEL WOUND DRESSING received FDA 510(k) clearance on 1995-01-12, under 510(k) number K945313.

Who is the listed applicant for SPARTA HYDROGEL WOUND DRESSING?

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 HYDROGEL WOUND DRESSING?

The FDA product code for SPARTA HYDROGEL WOUND DRESSING is MGQ.

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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-SDK922729SPARTA WET DRESSING, SODIUM CHLORIDEK905384DAVID SIMMONDS ANESTHESIA EXTENSION TUBESK905240VESSELOOPSK896085SURGI-BRUSHK896084MICROSPEARS

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Related Devices (Code: MGQ)

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K171879HylaGuard Moisturizing CreamFounders Science Group, LLCK083024HYLATOPIC EMOLLIENT FOAMCollegium Pharmaceutical IncorporatedK041342IMPRUV A.I. CREAM WOUND AND SKIN EMULSIONStiefel Laboratories, Inc.K041268SILVERSITE OR CALGITROLAdriK040019SILVERSEALNoble Fiber TechnologiesK040517TENDERWET ACTIVEMedline Industries, 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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