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FDA 510(k)

HEMOSTASYL PASTE

K-Number: K082116 · 2008-12-17

ApplicantSatelec
Decision Date2008-12-17
Product CodeMVL
DecisionSubstantially Equivalent

Device Summary

HEMOSTASYL PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Satelec. It received FDA 510(k) clearance on 2008-12-17 under 510(k) number K082116. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOSTASYL PASTE?

HEMOSTASYL PASTE is a medical device that received FDA 510(k) clearance on 2008-12-17. The listed applicant is Satelec. The 510(k) number is K082116.

When did HEMOSTASYL PASTE receive FDA 510(k) clearance?

HEMOSTASYL PASTE received FDA 510(k) clearance on 2008-12-17, under 510(k) number K082116.

Who is the listed applicant for HEMOSTASYL PASTE?

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

What is the FDA product code for HEMOSTASYL PASTE?

The FDA product code for HEMOSTASYL PASTE is MVL.

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.

Other records listing Satelec 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.

View all 24 devices →

Related Devices (Code: MVL)

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.

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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