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FDA 510(k)

QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350)

K-Number: K963552 · 1996-11-22

ApplicantTecnol Medical Products, Inc.
Decision Date1996-11-22
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350) is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol Medical Products, Inc.. It received FDA 510(k) clearance on 1996-11-22 under 510(k) number K963552. 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 QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350)?

QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350) is a medical device that received FDA 510(k) clearance on 1996-11-22. The listed applicant is Tecnol Medical Products, Inc.. The 510(k) number is K963552.

When did QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350) receive FDA 510(k) clearance?

QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350) received FDA 510(k) clearance on 1996-11-22, under 510(k) number K963552.

Who is the listed applicant for QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350)?

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

What is the FDA product code for QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350)?

The FDA product code for QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350) 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 Tecnol Medical Products, 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.

K974068PFR95 PARTICULATE FILTER RESPIRATOR AND SURGICAL MASK REGULAR SIZE, PFR95 PARTICULATE FILTER RESPIRATOR AND SURGICALK970448PCM 2000; ISOLAIR APR MODEL 2735K963564PERSONAL LIMB HOLDER (24444-200,300,24444-KIT)K963559WRPAROUND LIMB HOLDER (24446,24446-350,24447-010,24449-010)K963556SECURE-ALL 1-PIECE BODY HOLDER, SMALL/MEDIUM (24451-010,020,24452-010,020,030)K963557SYSTEM 2 ZIPPERED BODY HOLDER, SMALL/MEDIUM 24453-010,24453-020,24453-030

View all 21 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.

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