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)

KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING

K-Number: K973509 · 1997-12-04

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1997-12-04
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1997-12-04 under 510(k) number K973509. 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 KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING?

KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1997-12-04. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K973509.

When did KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING receive FDA 510(k) clearance?

KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING received FDA 510(k) clearance on 1997-12-04, under 510(k) number K973509.

Who is the listed applicant for KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING?

The FDA product code for KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING 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 Kendall Healthcare Products Co. Div.Of Tyco Health 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.

K973763KENDALL CURITY IODOFORM PACKING STRIPK973511KENDALL CURITY PETROLATUM GAUZEK973507KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)K973619KENDALL CURITY NON-ADHERING DRESSINGK973546KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETERK970266KENDALL HYDROPHILIC POWDER WOUND DRESSING

View all 66 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.

↑