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FDA 510(k)

MOLTENO VALVE SETON

K-Number: K875099 · 1988-03-30

ApplicantStaar Surgical Co.
Decision Date1988-03-30
Product CodeKYF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MOLTENO VALVE SETON is the device name listed in this FDA 510(k) record. The listed applicant is Staar Surgical Co.. It received FDA 510(k) clearance on 1988-03-30 under 510(k) number K875099. The device is classified under product code KYF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOLTENO VALVE SETON?

MOLTENO VALVE SETON is a medical device that received FDA 510(k) clearance on 1988-03-30. The listed applicant is Staar Surgical Co.. The 510(k) number is K875099.

When did MOLTENO VALVE SETON receive FDA 510(k) clearance?

MOLTENO VALVE SETON received FDA 510(k) clearance on 1988-03-30, under 510(k) number K875099.

Who is the listed applicant for MOLTENO VALVE SETON?

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

What is the FDA product code for MOLTENO VALVE SETON?

The FDA product code for MOLTENO VALVE SETON is KYF.

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Other records listing Staar Surgical Co. 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.

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Related Devices (Code: KYF)

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.

K230975Ahmed® Glaucoma Valve Model FP7New World Medical, Inc.K231051Ahmed® Glaucoma Valve Model FP8New World Medical, Inc.K220032iStent infinite Trabecular Micro-Bypass System, Model iS3Glaukos CorporationK182518AHMED ClearPath Glaucoma Drainage DeviceNew World Medical, Inc.K171451Ahmed Glaucoma Valve Model FP8New World Medical, Inc.K161457XEN Glaucoma Treatment SystemAllergan, 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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