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FDA 510(k)

LACERATION TRAY

K-Number: K963723 · 1996-11-27

ApplicantGrand Medical Products
Decision Date1996-11-27
Product CodeLRP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LACERATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Grand Medical Products. It received FDA 510(k) clearance on 1996-11-27 under 510(k) number K963723. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACERATION TRAY?

LACERATION TRAY is a medical device that received FDA 510(k) clearance on 1996-11-27. The listed applicant is Grand Medical Products. The 510(k) number is K963723.

When did LACERATION TRAY receive FDA 510(k) clearance?

LACERATION TRAY received FDA 510(k) clearance on 1996-11-27, under 510(k) number K963723.

Who is the listed applicant for LACERATION TRAY?

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

What is the FDA product code for LACERATION TRAY?

The FDA product code for LACERATION TRAY is LRP.

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 Grand Medical 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.

K963724GAUZE SPONGE, NON X-RAY DETECTABLEK963721SKIN SCRUB TRAYK963719CENTRAL LINE DRESSING CHANGE TRAY, TPN/CVP DRESSING CHANGE TRAYK963720TRACHEOSTOMY KITK963714GRAND MEDICAL SUTURE REMOVAL KITK963722IV START KIT

View all 8 devices →

Related Devices (Code: LRP)

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.

K951811OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACKOsteotech, Inc.K940239EYE TRAYCush Medical ProductsK935621CUSTOM ENT PACKSAssociated MedicalK940646ORTHOPEDIC TRAY PRODUCT LINECushinduK940444GENERAL SURGERY TRAYCush Medical ProductsK922126HOSPITAL KIT ENT 1125Savoy Medical Supply Co., 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.

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