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)

HYDRACARE ABSORBENT WOUND DRESSING

K-Number: K951914 · 1995-05-15

ApplicantAcacia Laboratories, Inc.
Decision Date1995-05-15
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

HYDRACARE ABSORBENT WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Acacia Laboratories, Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K951914. 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 HYDRACARE ABSORBENT WOUND DRESSING?

HYDRACARE ABSORBENT WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is Acacia Laboratories, Inc.. The 510(k) number is K951914.

When did HYDRACARE ABSORBENT WOUND DRESSING receive FDA 510(k) clearance?

HYDRACARE ABSORBENT WOUND DRESSING received FDA 510(k) clearance on 1995-05-15, under 510(k) number K951914.

Who is the listed applicant for HYDRACARE ABSORBENT WOUND DRESSING?

The FDA 510(k) record lists Acacia Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDRACARE ABSORBENT WOUND DRESSING?

The FDA product code for HYDRACARE ABSORBENT 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 Acacia Laboratories, Inc. 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.

K952419STERIGAUZE GEL DRESSINGK952420STERIGAUZE WET DRESSINGK951861STERICARE WOUND CARE GELK952414PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETERK950344HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETERK913408STERILE PLASTIC DRAPE

View all 12 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.

↑