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)

BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM

K-Number: K895207 · 1989-09-28

ApplicantJohnson & Johnson International
Decision Date1989-09-28
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson International. It received FDA 510(k) clearance on 1989-09-28 under 510(k) number K895207. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM?

BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM is a medical device that received FDA 510(k) clearance on 1989-09-28. The listed applicant is Johnson & Johnson International. The 510(k) number is K895207.

When did BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM receive FDA 510(k) clearance?

BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM received FDA 510(k) clearance on 1989-09-28, under 510(k) number K895207.

Who is the listed applicant for BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM?

The FDA 510(k) record lists Johnson & Johnson International as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM?

The FDA product code for BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM is FRO. This falls under the Anesthesiology category.

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 Johnson & Johnson International 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.

K965198ULTIMA TPS CEMENTED STEMK944937SYNTHETIC ABSORBABLE SUTUREK946245TIELLE* HYDROPOLYMER DRESSINGK942383DERMIVIEW CLEAR TAPEK922918BARRIER SAF-TE HYDROGEL DRAPEK923807P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS

View all 10 devices →

Related Devices (Code: FRO)

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.

K254168Actolind® (06.3637. Actolind® Gel Plus)ACTO GmbHK254041SkinSmart Antimicrobial HydroGelMagic Science Supply, LLCK261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.K253665Vashe Plus Antimicrobial SolutionUrgo Medical North America, LLCK251929SilverCeuticals® Antimicrobial Wound GelSilverceuticals, Inc.K261023Microdacyn Wound Irrigation SolutionSonoma Pharmaceuticals, 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.

↑