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)

ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET

K-Number: K973633 · 1998-01-16

ApplicantAtrion Medical Products, Inc.
Decision Date1998-01-16
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Atrion Medical Products, Inc.. It received FDA 510(k) clearance on 1998-01-16 under 510(k) number K973633. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET?

ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET is a medical device that received FDA 510(k) clearance on 1998-01-16. The listed applicant is Atrion Medical Products, Inc.. The 510(k) number is K973633.

When did ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET receive FDA 510(k) clearance?

ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET received FDA 510(k) clearance on 1998-01-16, under 510(k) number K973633.

Who is the listed applicant for ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET?

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

What is the FDA product code for ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET?

The FDA product code for ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET 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 Atrion Medical Products, 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.

K060643QL LOCKING SYRINGEK043249ATRION NEEDLEVISE LARGE-BORE SHARPS SECURING DEVICEK041158ATRION EPIDURAL ANESTHESIA KIT WITH ATRION NEEDLEVISE SHARPS SECURING SYSTEMK032840ATRION MEDICAL QL INFLATION DEVICEK020333ATRION MEDICAL QL FLUID DISPENSING SYRINGEK973872ATRION MEDICAL COATED LACRIMAL INTUBATION SET

View all 9 devices →

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.

↑