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FDA 510(k)

MIRACLELENS

K-Number: K770955 · 1977-06-17

ApplicantM.R.M. Optics, Inc.
Decision Date1977-06-17
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MIRACLELENS is the device name listed in this FDA 510(k) record. The listed applicant is M.R.M. Optics, Inc.. It received FDA 510(k) clearance on 1977-06-17 under 510(k) number K770955. 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 MIRACLELENS?

MIRACLELENS is a medical device that received FDA 510(k) clearance on 1977-06-17. The listed applicant is M.R.M. Optics, Inc.. The 510(k) number is K770955.

When did MIRACLELENS receive FDA 510(k) clearance?

MIRACLELENS received FDA 510(k) clearance on 1977-06-17, under 510(k) number K770955.

Who is the listed applicant for MIRACLELENS?

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

What is the FDA product code for MIRACLELENS?

The FDA product code for MIRACLELENS is HQG.

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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.K884360SEIKO P-6 PROGRESSIVE SPECTACLE LENSESSeiko Corp.K882814NEOLENS PRESCRIPTION SPECTACLE LENSNeolens, Inc.K882308CR-39 PLASTIC LENSES FOR EYEGLASSESAutomated Lens System

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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