Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN WOUND DRESSINGS

K-Number: K963598 · 1996-11-27

ApplicantInnovative Technologies , Ltd.
Decision Date1996-11-27
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN 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 1996-11-27 under 510(k) number K963598. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN WOUND DRESSINGS?

INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN WOUND DRESSINGS is a medical device that received FDA 510(k) clearance on 1996-11-27. The listed applicant is Innovative Technologies , Ltd.. The 510(k) number is K963598.

When did INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN WOUND DRESSINGS receive FDA 510(k) clearance?

INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN WOUND DRESSINGS received FDA 510(k) clearance on 1996-11-27, under 510(k) number K963598.

Who is the listed applicant for INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN 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 ALIGINATE/PECTIN WOUND DRESSINGS?

The FDA product code for INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K983303INNOVATIVE TECHNOLOGIES HYDROCOLLOID AND INTELLIGENT HYDROCOLLOID WOUND DRESSINGSK982234AL-GEN CALCIUM ALGINATE DRESSINGK9826383M TEGAGEN HI ALGINATE DRESSING & 3 M TEGAGEN HG ALGINATE DRESSING, MODEL #'S 90110,90112,90114,90120, 90210,90212,90214K981753INNOVATIVE TECHNOLOGIES TRANSPARENT FILM AND INTELLIGENT FILM WOUND DRESSINGK9809893M TEGAGEN HI ALGINATE DRESSING & 3M TEGAGEN HG ALGINATE DRESSINGK980097FLEXIGEL-G HYDROGEL WOUND DRESSING

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, Inc.

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.

↑