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FDA 510(k)

NOSITE UV INTERIM SPECTACLES

K-Number: K823825 · 1983-02-24

ApplicantPatton, Boggs & Blow
Decision Date1983-02-24
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NOSITE UV INTERIM SPECTACLES is the device name listed in this FDA 510(k) record. The listed applicant is Patton, Boggs & Blow. It received FDA 510(k) clearance on 1983-02-24 under 510(k) number K823825. 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 NOSITE UV INTERIM SPECTACLES?

NOSITE UV INTERIM SPECTACLES is a medical device that received FDA 510(k) clearance on 1983-02-24. The listed applicant is Patton, Boggs & Blow. The 510(k) number is K823825.

When did NOSITE UV INTERIM SPECTACLES receive FDA 510(k) clearance?

NOSITE UV INTERIM SPECTACLES received FDA 510(k) clearance on 1983-02-24, under 510(k) number K823825.

Who is the listed applicant for NOSITE UV INTERIM SPECTACLES?

The FDA 510(k) record lists Patton, Boggs & Blow as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOSITE UV INTERIM SPECTACLES?

The FDA product code for NOSITE UV INTERIM SPECTACLES is HQG.

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Other records listing Patton, Boggs & Blow 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.

K943347KLS MINI OSTEOSYNTHESIS SYSTEMK943346MANUAL SURGICAL INST. AND ACC. TO KLS MINI OSTEOSYNTHESIS SYSTEMK943348KLS CHIN PLATE SYSTEMK943345MANUAL SURGICAL INST. AND ACC. TO KLS CHIN PLATE SYSTEMK821799FITKIT I CHECKUP KIT

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

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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