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FDA 510(k)

JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE

K-Number: K950869 · 1995-10-27

Decision Date1995-10-27
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Jobar Intl., Inc.. It received FDA 510(k) clearance on 1995-10-27 under 510(k) number K950869. 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 JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE?

JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1995-10-27. The listed applicant is Jobar Intl., Inc.. The 510(k) number is K950869.

When did JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE receive FDA 510(k) clearance?

JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE received FDA 510(k) clearance on 1995-10-27, under 510(k) number K950869.

Who is the listed applicant for JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE?

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

What is the FDA product code for JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE?

The FDA product code for JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE is LRX.

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.

Related Devices (Code: LRX)

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.

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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