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FDA 510(k)

OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE

K-Number: K875197 · 1988-02-09

ApplicantPro-Optics, Inc.
Decision Date1988-02-09
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Optics, Inc.. It received FDA 510(k) clearance on 1988-02-09 under 510(k) number K875197. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE?

OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE is a medical device that received FDA 510(k) clearance on 1988-02-09. The listed applicant is Pro-Optics, Inc.. The 510(k) number is K875197.

When did OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE receive FDA 510(k) clearance?

OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE received FDA 510(k) clearance on 1988-02-09, under 510(k) number K875197.

Who is the listed applicant for OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE?

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

What is the FDA product code for OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE?

The FDA product code for OPTIK-AIDS/OPTIC-SHOP THERMAL/THERMA PRO LENS CASE is LRX.

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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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