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FDA 510(k)

SEIKO P-6 PROGRESSIVE SPECTACLE LENSES

K-Number: K884360 · 1988-11-15

ApplicantSeiko Corp.
Decision Date1988-11-15
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SEIKO P-6 PROGRESSIVE SPECTACLE LENSES is the device name listed in this FDA 510(k) record. The listed applicant is Seiko Corp.. It received FDA 510(k) clearance on 1988-11-15 under 510(k) number K884360. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEIKO P-6 PROGRESSIVE SPECTACLE LENSES?

SEIKO P-6 PROGRESSIVE SPECTACLE LENSES is a medical device that received FDA 510(k) clearance on 1988-11-15. The listed applicant is Seiko Corp.. The 510(k) number is K884360.

When did SEIKO P-6 PROGRESSIVE SPECTACLE LENSES receive FDA 510(k) clearance?

SEIKO P-6 PROGRESSIVE SPECTACLE LENSES received FDA 510(k) clearance on 1988-11-15, under 510(k) number K884360.

Who is the listed applicant for SEIKO P-6 PROGRESSIVE SPECTACLE LENSES?

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

What is the FDA product code for SEIKO P-6 PROGRESSIVE SPECTACLE LENSES?

The FDA product code for SEIKO P-6 PROGRESSIVE SPECTACLE LENSES is HQG.

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.

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Other records listing Seiko 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.

K900732SPECTACLE FRAME

Related Devices (Code: HQG)

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.

K935919SUNGLASSESJa-Ru, Inc.K9207950R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEXOptical Radiation Corp.K900091MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOROnufryk Low Vision Ent.K882814NEOLENS PRESCRIPTION SPECTACLE LENSNeolens, Inc.K882308CR-39 PLASTIC LENSES FOR EYEGLASSESAutomated Lens SystemK881225OPHTHALMIC SPECTACLE LENS BLANKSBeta Optical Co, 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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