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FDA 510(k)

ALGINATE FIBER

K-Number: K941176 · 1994-07-28

ApplicantAdri/Technam
Decision Date1994-07-28
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

ALGINATE FIBER is the device name listed in this FDA 510(k) record. The listed applicant is Adri/Technam. It received FDA 510(k) clearance on 1994-07-28 under 510(k) number K941176. 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 ALGINATE FIBER?

ALGINATE FIBER is a medical device that received FDA 510(k) clearance on 1994-07-28. The listed applicant is Adri/Technam. The 510(k) number is K941176.

When did ALGINATE FIBER receive FDA 510(k) clearance?

ALGINATE FIBER received FDA 510(k) clearance on 1994-07-28, under 510(k) number K941176.

Who is the listed applicant for ALGINATE FIBER?

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

What is the FDA product code for ALGINATE FIBER?

The FDA product code for ALGINATE FIBER 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 Adri/Technam 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.

K003134FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSINGK914779ALGINATE FIBER

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.

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