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)

LOOK IRRIGATING/ASPIRATING CANNULAS

K-Number: K870436 · 1987-02-20

ApplicantLook, Inc.
Decision Date1987-02-20
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LOOK IRRIGATING/ASPIRATING CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Look, Inc.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K870436. The device is classified under product code HMX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOOK IRRIGATING/ASPIRATING CANNULAS?

LOOK IRRIGATING/ASPIRATING CANNULAS is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Look, Inc.. The 510(k) number is K870436.

When did LOOK IRRIGATING/ASPIRATING CANNULAS receive FDA 510(k) clearance?

LOOK IRRIGATING/ASPIRATING CANNULAS received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870436.

Who is the listed applicant for LOOK IRRIGATING/ASPIRATING CANNULAS?

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

What is the FDA product code for LOOK IRRIGATING/ASPIRATING CANNULAS?

The FDA product code for LOOK IRRIGATING/ASPIRATING CANNULAS is HMX.

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 Look, 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.

K943949POLYVIOLENE SURGICL SUTUREK933686LOOK INC. 316L STAINLESS STEEL SURGICAL SUTUREK926586REVISED LABELING FOR CHROMIC AND PLAIN GUT SUTURESK926168SILK SUTURES-REVISED LABELINGK926167POLYVIOLENE SUTURE-REVISED LABELINGK926587REVISED LABELING FOR NYLON SUTURE (POLYAMIDE)

View all 25 devices →

Related Devices (Code: HMX)

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.

K010305WEISS RETINAL CANNULAMicron Surgical, Inc.K000457VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIESRetinalabs.ComK970873ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)American Medical Devices, Inc.K943932STERISEAL OPHTHALMIC CANNULAPharma-Plast, Ltd.K942403INFUSION CANNULAMicrosurgical Technology, Inc.K934844INTER TIP TMicrosurgical Technology, 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.

↑