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)

PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957)

K-Number: K924834 · 1993-03-23

ApplicantAmerican Healthcare Supply Co., Inc.
Decision Date1993-03-23
Product CodeMCZ
Advisory CommitteeSU
DecisionUnknown

Device Summary

PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957) is the device name listed in this FDA 510(k) record. The listed applicant is American Healthcare Supply Co., Inc.. It received FDA 510(k) clearance on 1993-03-23 under 510(k) number K924834. The device is classified under product code MCZ. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957)?

PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957) is a medical device that received FDA 510(k) clearance on 1993-03-23. The listed applicant is American Healthcare Supply Co., Inc.. The 510(k) number is K924834.

When did PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957) receive FDA 510(k) clearance?

PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957) received FDA 510(k) clearance on 1993-03-23, under 510(k) number K924834.

Who is the listed applicant for PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957)?

The FDA 510(k) record lists American Healthcare Supply Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957)?

The FDA product code for PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957) 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 American Healthcare Supply Co., 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.

K925214SHAVE PREP TRAYS (NON-STERILE)K925216STERILE SKIN SCRUB TRAYSK925215STERILE SURGICAL INSTRUMENT TRAYSK924835VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560

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.K963714GRAND MEDICAL SUTURE REMOVAL KITGrand Medical ProductsK943046SKIN STAPLE REMOVAL TRAYSSterile Concepts, Inc.K941465SUTURE REMOVAL KITClinical Resources, Inc.K931597CARAPACE INCISION AND DRAINAGE TRAYSCarapace, 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.

↑