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FDA 510(k)

QUICKCLOT

K-Number: K013390 · 2002-05-23

ApplicantOn Site Gas Systems, Inc.
Decision Date2002-05-23
Product CodeQSY
DecisionSubstantially Equivalent

Device Summary

QUICKCLOT is the device name listed in this FDA 510(k) record. The listed applicant is On Site Gas Systems, Inc.. It received FDA 510(k) clearance on 2002-05-23 under 510(k) number K013390. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKCLOT?

QUICKCLOT is a medical device that received FDA 510(k) clearance on 2002-05-23. The listed applicant is On Site Gas Systems, Inc.. The 510(k) number is K013390.

When did QUICKCLOT receive FDA 510(k) clearance?

QUICKCLOT received FDA 510(k) clearance on 2002-05-23, under 510(k) number K013390.

Who is the listed applicant for QUICKCLOT?

The FDA 510(k) record lists On Site Gas Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICKCLOT?

The FDA product code for QUICKCLOT is QSY.

Related Clinical Trials

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.

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Other records listing On Site Gas Systems, 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.

K092636POGS, MODEL 65/130K063454POGS, MODEL 33CK041664PORTABLE OXYGEN GENERATION SYSTEM: POGS 33CK030920POGS 33K021581HEMOSORBK021082ON SITE GAS SYSTEMS PORTABLE OXYGEN GENERATION SYSTEM-1.0 AND 5.0

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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

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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