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)

A.C.S. SUTURE REMOVAL KIT

K-Number: K915827 · 1992-12-08

ApplicantAmerican Carolina Stamping
Decision Date1992-12-08
Product CodeMCZ
Advisory CommitteeSU
DecisionUnknown

Device Summary

A.C.S. SUTURE REMOVAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Carolina Stamping. It received FDA 510(k) clearance on 1992-12-08 under 510(k) number K915827. 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 A.C.S. SUTURE REMOVAL KIT?

A.C.S. SUTURE REMOVAL KIT is a medical device that received FDA 510(k) clearance on 1992-12-08. The listed applicant is American Carolina Stamping. The 510(k) number is K915827.

When did A.C.S. SUTURE REMOVAL KIT receive FDA 510(k) clearance?

A.C.S. SUTURE REMOVAL KIT received FDA 510(k) clearance on 1992-12-08, under 510(k) number K915827.

Who is the listed applicant for A.C.S. SUTURE REMOVAL KIT?

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

What is the FDA product code for A.C.S. SUTURE REMOVAL KIT?

The FDA product code for A.C.S. 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

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.

↑