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)

PROD NO. 01-1694 - 4X4 FOAM DRESSING

K-Number: K954728 · 1996-09-23

ApplicantContinental Medical Laboratories, Inc.
Decision Date1996-09-23
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

PROD NO. 01-1694 - 4X4 FOAM DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Continental Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1996-09-23 under 510(k) number K954728. 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 PROD NO. 01-1694 - 4X4 FOAM DRESSING?

PROD NO. 01-1694 - 4X4 FOAM DRESSING is a medical device that received FDA 510(k) clearance on 1996-09-23. The listed applicant is Continental Medical Laboratories, Inc.. The 510(k) number is K954728.

When did PROD NO. 01-1694 - 4X4 FOAM DRESSING receive FDA 510(k) clearance?

PROD NO. 01-1694 - 4X4 FOAM DRESSING received FDA 510(k) clearance on 1996-09-23, under 510(k) number K954728.

Who is the listed applicant for PROD NO. 01-1694 - 4X4 FOAM DRESSING?

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

What is the FDA product code for PROD NO. 01-1694 - 4X4 FOAM DRESSING?

The FDA product code for PROD NO. 01-1694 - 4X4 FOAM 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 Continental Medical 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.

K964827PROD. NO. 01-132 - SUTURE REMOVAL KITK963234STAPLE REMOVAL KITK963443PROD. NO. 02-031 - LACERATION TRAYK962078TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETERK962073URETHRAL CATHETERIZATION TRAY/UNIVERSAL URETHRAL CATH TRAYK952335WOUND CARE MANAGEMENT KITS

View all 8 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.

↑