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FDA 510(k)

OPHTHALMIC CANNULA

K-Number: K881487 · 1988-04-29

ApplicantSurgical Instrument, Inc.
Decision Date1988-04-29
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instrument, Inc.. It received FDA 510(k) clearance on 1988-04-29 under 510(k) number K881487. 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 OPHTHALMIC CANNULA?

OPHTHALMIC CANNULA is a medical device that received FDA 510(k) clearance on 1988-04-29. The listed applicant is Surgical Instrument, Inc.. The 510(k) number is K881487.

When did OPHTHALMIC CANNULA receive FDA 510(k) clearance?

OPHTHALMIC CANNULA received FDA 510(k) clearance on 1988-04-29, under 510(k) number K881487.

Who is the listed applicant for OPHTHALMIC CANNULA?

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

What is the FDA product code for OPHTHALMIC CANNULA?

The FDA product code for OPHTHALMIC CANNULA 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 Surgical Instrument, 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.

K930607GRIPPERK923667IRRIGATION/SUCTION PROBE

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.

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