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FDA 510(k)

COLLIEVA

K-Number: K081782 · 2008-09-30

Decision Date2008-09-30
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

COLLIEVA is the device name listed in this FDA 510(k) record. The listed applicant is Innocoll Pharmaceuticals. It received FDA 510(k) clearance on 2008-09-30 under 510(k) number K081782. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLIEVA?

COLLIEVA is a medical device that received FDA 510(k) clearance on 2008-09-30. The listed applicant is Innocoll Pharmaceuticals. The 510(k) number is K081782.

When did COLLIEVA receive FDA 510(k) clearance?

COLLIEVA received FDA 510(k) clearance on 2008-09-30, under 510(k) number K081782.

Who is the listed applicant for COLLIEVA?

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

What is the FDA product code for COLLIEVA?

The FDA product code for COLLIEVA is KGN.

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 Innocoll Pharmaceuticals 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.

Related Devices (Code: KGN)

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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