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FDA 510(k)

BIOPAD

K-Number: K040283 · 2005-07-22

ApplicantEuroresearch Srl
Decision Date2005-07-22
Product CodeQSY
DecisionSubstantially Equivalent

Device Summary

BIOPAD is the device name listed in this FDA 510(k) record. The listed applicant is Euroresearch Srl. It received FDA 510(k) clearance on 2005-07-22 under 510(k) number K040283. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPAD?

BIOPAD is a medical device that received FDA 510(k) clearance on 2005-07-22. The listed applicant is Euroresearch Srl. The 510(k) number is K040283.

When did BIOPAD receive FDA 510(k) clearance?

BIOPAD received FDA 510(k) clearance on 2005-07-22, under 510(k) number K040283.

Who is the listed applicant for BIOPAD?

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

What is the FDA product code for BIOPAD?

The FDA product code for BIOPAD is QSY.

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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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