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)

MEDLINE ZIPPER SLEEVED VEST

K-Number: K963452 · 1996-10-18

ApplicantMedline
Decision Date1996-10-18
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDLINE ZIPPER SLEEVED VEST is the device name listed in this FDA 510(k) record. The listed applicant is Medline. It received FDA 510(k) clearance on 1996-10-18 under 510(k) number K963452. The device is classified under product code FMQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE ZIPPER SLEEVED VEST?

MEDLINE ZIPPER SLEEVED VEST is a medical device that received FDA 510(k) clearance on 1996-10-18. The listed applicant is Medline. The 510(k) number is K963452.

When did MEDLINE ZIPPER SLEEVED VEST receive FDA 510(k) clearance?

MEDLINE ZIPPER SLEEVED VEST received FDA 510(k) clearance on 1996-10-18, under 510(k) number K963452.

Who is the listed applicant for MEDLINE ZIPPER SLEEVED VEST?

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

What is the FDA product code for MEDLINE ZIPPER SLEEVED VEST?

The FDA product code for MEDLINE ZIPPER SLEEVED VEST is FMQ.

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 Medline 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.

K120156PUREIMAGE ULTRASOUND TRANSMISSION GELK051378POWDER-FREE BLUE NITRILE EXAMINATION GLOVES (TESTED FOR USE WITH CHEMOTHERAPY DRUGS)K010825MEDLINE STERISET STERILIZATION CONTAINERK990463MEDLINE EXCEL WHEELCHAIRSK970282MEDLINE CIRCUMCISION TRAYK963504MEDLINE OPEN END FINGER CONTROL MITT

View all 11 devices →

Related Devices (Code: FMQ)

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.

K110377PROTECTIVE RESTRAINTMedi-Tech Intl. Corp.K081264STATSTRAP NEONATAL INCUBATOR SAFETY STRAP, MODELS SS-001, SS-002Children'S Health First, Inc.K080448CENTURION PROTECTIVE RESTRAINT, SCR SERIESTri-State Hospital Supply Corp.K013239COMFORTCARE COMPRESSION SUPPORT WITH MAGNETS COMFORTCARE MAGNETIC INSOLESMed Gen, Inc.K010818INFANT LIMB HOLDER, MODELS 306080 & 306081Skil-Care Corp.K010644CINCH-TYPE DISPOSABLE LIMB HOLDERS, MODEL 912025Skil-Care Corp.

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.

↑