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)

CARAPACE INCISION AND DRAINAGE TRAYS

K-Number: K931597 · 1993-11-05

ApplicantCarapace, Inc.
Decision Date1993-11-05
Product CodeMCZ
Advisory CommitteeSU
DecisionUnknown

Device Summary

CARAPACE INCISION AND DRAINAGE TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Carapace, Inc.. It received FDA 510(k) clearance on 1993-11-05 under 510(k) number K931597. 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 CARAPACE INCISION AND DRAINAGE TRAYS?

CARAPACE INCISION AND DRAINAGE TRAYS is a medical device that received FDA 510(k) clearance on 1993-11-05. The listed applicant is Carapace, Inc.. The 510(k) number is K931597.

When did CARAPACE INCISION AND DRAINAGE TRAYS receive FDA 510(k) clearance?

CARAPACE INCISION AND DRAINAGE TRAYS received FDA 510(k) clearance on 1993-11-05, under 510(k) number K931597.

Who is the listed applicant for CARAPACE INCISION AND DRAINAGE TRAYS?

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

What is the FDA product code for CARAPACE INCISION AND DRAINAGE TRAYS?

The FDA product code for CARAPACE INCISION AND DRAINAGE TRAYS 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 Carapace, 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.

K931722CARAPACE LABOR AND DELIVERY SETSK931822CARAPACE PELVIC EXAM TRAYSK931729I.V. START KITK931669CARAPACE DEBRIDEMENT KITSK931820CARAPACE STILLWATER BOWL SETK931760CARAPACE PACKING GAUZE TRAYS

View all 22 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.K963714GRAND MEDICAL SUTURE REMOVAL KITGrand Medical ProductsK943046SKIN STAPLE REMOVAL TRAYSSterile Concepts, Inc.K941465SUTURE REMOVAL KITClinical Resources, 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.

↑