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FDA 510(k)

OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)

K-Number: K952260 · 1996-01-03

Decision Date1996-01-03
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C) is the device name listed in this FDA 510(k) record. The listed applicant is Stellar Contact Lens, Inc.. It received FDA 510(k) clearance on 1996-01-03 under 510(k) number K952260. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)?

OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C) is a medical device that received FDA 510(k) clearance on 1996-01-03. The listed applicant is Stellar Contact Lens, Inc.. The 510(k) number is K952260.

When did OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C) receive FDA 510(k) clearance?

OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C) received FDA 510(k) clearance on 1996-01-03, under 510(k) number K952260.

Who is the listed applicant for OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)?

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

What is the FDA product code for OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)?

The FDA product code for OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C) is HQD.

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: HQD)

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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