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FDA 510(k)

MEDTRADE PRODUCTS CELOX TRAUMA GAUZE

K-Number: K091795 · 2009-11-20

ApplicantMedtrade Products , Ltd.
Decision Date2009-11-20
Product CodeQSY
DecisionSubstantially Equivalent

Device Summary

MEDTRADE PRODUCTS CELOX TRAUMA GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Medtrade Products , Ltd.. It received FDA 510(k) clearance on 2009-11-20 under 510(k) number K091795. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRADE PRODUCTS CELOX TRAUMA GAUZE?

MEDTRADE PRODUCTS CELOX TRAUMA GAUZE is a medical device that received FDA 510(k) clearance on 2009-11-20. The listed applicant is Medtrade Products , Ltd.. The 510(k) number is K091795.

When did MEDTRADE PRODUCTS CELOX TRAUMA GAUZE receive FDA 510(k) clearance?

MEDTRADE PRODUCTS CELOX TRAUMA GAUZE received FDA 510(k) clearance on 2009-11-20, under 510(k) number K091795.

Who is the listed applicant for MEDTRADE PRODUCTS CELOX TRAUMA GAUZE?

The FDA 510(k) record lists Medtrade Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDTRADE PRODUCTS CELOX TRAUMA GAUZE?

The FDA product code for MEDTRADE PRODUCTS CELOX TRAUMA GAUZE is QSY.

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Other records listing Medtrade Products , Ltd. 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.

K230589Celox Rapid X-Ray GauzeK161274Bondiloxs Topical Hemostatic GranulesK120930CHG ANTIBACTERIAL FOAM DRESSING, CHG ANTIBACTERIAL PATCH, CHG ANTIBACTERIAL FOAM PATCH, CHG PATCH, CHG DRESSINGK113560CELOX GAUZE PROK110386CELOX RAPID GAUZEK102965CELOX TRAUMA GAUZE AG, CELOX HEMOSTATIC ANTIBACTERIAL TRAUMA GAUZE, OMNI-STAT TRAUMA GAUZE AG, OMNI-STAT HEMOSTATIC ANTI

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Related Devices (Code: QSY)

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.

K253017BloodSTOP iX Trauma Matrix (TM-iX-20)Lifescience Plus, Inc.K251700Ganymede 2cm diameter (FG100300); Ganymede 5cm x 5cm (FG100400); Ganymede 10cm x 10cm (FG100500); Ganymede 15cm x 15cm (FG100600); Ganymede 20cm x 30cm (FG100700); Ganymede 25cm x 25cm (FG100800); Ganymede 30cm x 30cm (FG100900); Ganymede 40cm x 40cm (FG100999); Ganymede 7.5cm x 120cm (FG100100); Ganymede-X 2cm diameter (FG100301); Ganymede-X 5cm x 5cm (FG100401); Ganymede-X 10cm x 10cm (FG100501); Ganymede-X 15cm x 15cm (FG100601); Ganymede-X 20cm x 30cm (FG100701); Ganymede-X 25cmSpeciality Fibres and Materials LimitedK250319MFUSE (MS001)Machina Medical, Inc.K253609TRAUMAGEL® 2.0 Hemostatic GelCresilon, Inc.K240713TRAUMAGEL®Cresilon, Inc.K240097Polysaccharide Hemostatic Powder (HP-2, HP-3, HP-5)Ushare Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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