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)

ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET

K-Number: K844199 · 1984-11-07

ApplicantKleen Test Products
Decision Date1984-11-07
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET is the device name listed in this FDA 510(k) record. The listed applicant is Kleen Test Products. It received FDA 510(k) clearance on 1984-11-07 under 510(k) number K844199. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET?

ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET is a medical device that received FDA 510(k) clearance on 1984-11-07. The listed applicant is Kleen Test Products. The 510(k) number is K844199.

When did ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET receive FDA 510(k) clearance?

ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET received FDA 510(k) clearance on 1984-11-07, under 510(k) number K844199.

Who is the listed applicant for ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET?

The FDA 510(k) record lists Kleen Test Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET?

The FDA product code for ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET is KKX.

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 Kleen Test Products 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.

K890039KLEEN TEST BASIN SETK890539SURE COUNT LIGHT HANDLE COVERK890098KLEEN TEST O.R. KITK853622SURE COUNT 30 COUNT FOAM & MAGNETIC 92-3030K853454SURE COUNT 5 & 10 SPONGE COUNTERK853315CAUTERY TIP CLEANING PAD

View all 17 devices →

Related Devices (Code: KKX)

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.

K230645BeneHold™ Surgical Incise Drape with CHG antimicrobial IIAvery Dennison Medical , Ltd.K2225783M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)3M CompanyK202208BeneHold Surgical Incise Drape with CHG antimicrobialAvery Dennison Belgie BvbaK200238ControlRad Sterile CoverControlrad, Inc.K163556MediClear PreOpCovalontechnologies, Inc.K130404TIBURON SURGICAL DRAPECardinal Health200, LLC

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.

↑