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FDA 510(k)

INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS

K-Number: K953781 · 1995-09-01

Decision Date1995-09-01
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Technologies , Ltd.. It received FDA 510(k) clearance on 1995-09-01 under 510(k) number K953781. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS?

INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS is a medical device that received FDA 510(k) clearance on 1995-09-01. The listed applicant is Innovative Technologies , Ltd.. The 510(k) number is K953781.

When did INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS receive FDA 510(k) clearance?

INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS received FDA 510(k) clearance on 1995-09-01, under 510(k) number K953781.

Who is the listed applicant for INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS?

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

What is the FDA product code for INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS?

The FDA product code for INNOVATIVE TECHNOLOGIES CALCIUM ALGINATE WOUND DRESSINGS is KMF.

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 Innovative Technologies , Ltd. 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 14 devices →

Related Devices (Code: KMF)

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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