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)

FERRIS POLYOSTOMY STERILE WOUND DRESSING

K-Number: K991729 · 1999-08-27

ApplicantFerris Mfg. Corp.
Decision Date1999-08-27
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FERRIS POLYOSTOMY STERILE WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Ferris Mfg. Corp.. It received FDA 510(k) clearance on 1999-08-27 under 510(k) number K991729. 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 FERRIS POLYOSTOMY STERILE WOUND DRESSING?

FERRIS POLYOSTOMY STERILE WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1999-08-27. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K991729.

When did FERRIS POLYOSTOMY STERILE WOUND DRESSING receive FDA 510(k) clearance?

FERRIS POLYOSTOMY STERILE WOUND DRESSING received FDA 510(k) clearance on 1999-08-27, under 510(k) number K991729.

Who is the listed applicant for FERRIS POLYOSTOMY STERILE WOUND DRESSING?

The FDA 510(k) record lists Ferris Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FERRIS POLYOSTOMY STERILE WOUND DRESSING?

The FDA product code for FERRIS POLYOSTOMY STERILE 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 Ferris Mfg. Corp. 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.

K031660FERRIS POLYMEM STERILE BREAST PADK031307FERRIS POLYMEM SILVER WOUND DRESSINGK002129FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGENK990906FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLERK984539FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSINGK982306POLYTUBE

View all 20 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.

↑