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FDA 510(k)

HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM

K-Number: K990086 · 1999-03-31

Decision Date1999-03-31
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM is the device name listed in this FDA 510(k) record. The listed applicant is Integra Lifesciences Corp.. It received FDA 510(k) clearance on 1999-03-31 under 510(k) number K990086. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM?

HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM is a medical device that received FDA 510(k) clearance on 1999-03-31. The listed applicant is Integra Lifesciences Corp.. The 510(k) number is K990086.

When did HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM receive FDA 510(k) clearance?

HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM received FDA 510(k) clearance on 1999-03-31, under 510(k) number K990086.

Who is the listed applicant for HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM?

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

What is the FDA product code for HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM?

The FDA product code for HELIDERM COLLAGEN WOUND DRESSINGS 0.5 GRAM AND 1.0 GRAM 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 Integra Lifesciences Corp. 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 27 devices →

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

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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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