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)

IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS

K-Number: K112702 · 2012-03-29

ApplicantImperial Surgical , Ltd.
Decision Date2012-03-29
Product CodeLGZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS is the device name listed in this FDA 510(k) record. The listed applicant is Imperial Surgical , Ltd.. It received FDA 510(k) clearance on 2012-03-29 under 510(k) number K112702. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS?

IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS is a medical device that received FDA 510(k) clearance on 2012-03-29. The listed applicant is Imperial Surgical , Ltd.. The 510(k) number is K112702.

When did IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS receive FDA 510(k) clearance?

IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS received FDA 510(k) clearance on 2012-03-29, under 510(k) number K112702.

Who is the listed applicant for IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS?

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

What is the FDA product code for IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS?

The FDA product code for IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS is LGZ.

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: LGZ)

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.

K262532NORMOFLO™ Irrigation Fluid Warming Sets and Accessories (IR-601, IR-501, IR-61, PL-61)ICU MedicalK260988°M Warmer System with °M StationMequ A/SK252636Fluido Compact SystemThe Surgical Company International B.V.K251733Fluido® AirGuard SystemThe Surgical Company International BV (As Tsc Life)K232107°M Warmer SystemMequ A/SK211618Fluido Compact Blood and Fluid Warming SystemThe Surgical Company International B.V.

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.

↑