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FDA 510(k)

CRAWFORD BIOCANALICULUS INTUBATION

K-Number: K121142 · 2012-08-09

ApplicantFci Sas (France Chirurgie Instrumentation)
Decision Date2012-08-09
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

CRAWFORD BIOCANALICULUS INTUBATION is the device name listed in this FDA 510(k) record. The listed applicant is Fci Sas (France Chirurgie Instrumentation). It received FDA 510(k) clearance on 2012-08-09 under 510(k) number K121142. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRAWFORD BIOCANALICULUS INTUBATION?

CRAWFORD BIOCANALICULUS INTUBATION is a medical device that received FDA 510(k) clearance on 2012-08-09. The listed applicant is Fci Sas (France Chirurgie Instrumentation). The 510(k) number is K121142.

When did CRAWFORD BIOCANALICULUS INTUBATION receive FDA 510(k) clearance?

CRAWFORD BIOCANALICULUS INTUBATION received FDA 510(k) clearance on 2012-08-09, under 510(k) number K121142.

Who is the listed applicant for CRAWFORD BIOCANALICULUS INTUBATION?

The FDA 510(k) record lists Fci Sas (France Chirurgie Instrumentation) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRAWFORD BIOCANALICULUS INTUBATION?

The FDA product code for CRAWFORD BIOCANALICULUS INTUBATION is OKS.

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 Fci Sas (France Chirurgie Instrumentation) 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.

K130375SELF-RETAINING BICANALICULUS INTUBATON SET IIK113536MASTERKA 40 MASTERKA 35 MASTERKA 30

Related Devices (Code: OKS)

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.

K201892Ritleng®+ and Ritleng®+ PVPFci (France Chirurgie Instrumentation) SasK201606LacriJet®Fci (France Chirurgie Instrumentation) SasK170247Lacriflow CLKaneka Pharma America, LLCK161373NunchakuFci (France Chirurgie Instrumentation)K160710Oasis Lacrimal Intubation SetAnodyneK130375SELF-RETAINING BICANALICULUS INTUBATON SET IIFci Sas (France Chirurgie Instrumentation)

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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