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FDA 510(k)

TAMCENAN OCULAR EXPLANTS AND BANDS

K-Number: K902308 · 1990-06-19

ApplicantTamcenan Corp.
Decision Date1990-06-19
Product CodeHQX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TAMCENAN OCULAR EXPLANTS AND BANDS is the device name listed in this FDA 510(k) record. The listed applicant is Tamcenan Corp.. It received FDA 510(k) clearance on 1990-06-19 under 510(k) number K902308. The device is classified under product code HQX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAMCENAN OCULAR EXPLANTS AND BANDS?

TAMCENAN OCULAR EXPLANTS AND BANDS is a medical device that received FDA 510(k) clearance on 1990-06-19. The listed applicant is Tamcenan Corp.. The 510(k) number is K902308.

When did TAMCENAN OCULAR EXPLANTS AND BANDS receive FDA 510(k) clearance?

TAMCENAN OCULAR EXPLANTS AND BANDS received FDA 510(k) clearance on 1990-06-19, under 510(k) number K902308.

Who is the listed applicant for TAMCENAN OCULAR EXPLANTS AND BANDS?

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

What is the FDA product code for TAMCENAN OCULAR EXPLANTS AND BANDS?

The FDA product code for TAMCENAN OCULAR EXPLANTS AND BANDS is HQX.

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 Tamcenan Corp. 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.

K905750LACRIMAL PLUGK901618OCULAR INFUSION CANNULA SYSTEM

Related Devices (Code: HQX)

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.

K023481MICROVISION SCLERAL BUCKLING COMPONENTSMicrovision, Inc.K983581OCU-GUARD AND OCU-GUARD SUPPLEBio-Vascular, Inc.K980816RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGESFci Ophthalmics, Inc.K963219RETINAL DETACHMENT IMPLANTS; INCLUDING BANS, STRIPS, TIRES, SLEEVES, CORDS AND SPONGESFci Ophthalmics, Inc.K950806SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTSMira, Inc.K950599STORS SCLERAL SPONGE II (LINCOFF DESIGN)Storz Ophthalmics, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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