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FDA 510(k)

GRAND MEDICAL SUTURE REMOVAL KIT

K-Number: K963714 · 1996-11-27

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

Device Summary

GRAND MEDICAL SUTURE REMOVAL KIT 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 K963714. The device is classified under product code MCZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAND MEDICAL SUTURE REMOVAL KIT?

GRAND MEDICAL SUTURE REMOVAL KIT 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 K963714.

When did GRAND MEDICAL SUTURE REMOVAL KIT receive FDA 510(k) clearance?

GRAND MEDICAL SUTURE REMOVAL KIT received FDA 510(k) clearance on 1996-11-27, under 510(k) number K963714.

Who is the listed applicant for GRAND MEDICAL SUTURE REMOVAL KIT?

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 GRAND MEDICAL SUTURE REMOVAL KIT?

The FDA product code for GRAND MEDICAL SUTURE REMOVAL KIT is MCZ.

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 DETECTABLEK963723LACERATION TRAYK963721SKIN SCRUB TRAYK963719CENTRAL LINE DRESSING CHANGE TRAY, TPN/CVP DRESSING CHANGE TRAYK963720TRACHEOSTOMY KITK963722IV START KIT

View all 8 devices →

Related Devices (Code: MCZ)

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.

K050656AMSINO SUTURE REMOVAL KITAmsino International, Inc.K964827PROD. NO. 01-132 - SUTURE REMOVAL KITContinental Medical Laboratories, Inc.K943046SKIN STAPLE REMOVAL TRAYSSterile Concepts, Inc.K941465SUTURE REMOVAL KITClinical Resources, Inc.K931597CARAPACE INCISION AND DRAINAGE TRAYSCarapace, Inc.K925015STERILE SUTURE REMOVAL KITCustomed, 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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