OP-2 (LOTIFOCON B) & OP-6 (LOTIFOCON C)
K-Number: K952260 · 1996-01-03
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Device Summary
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
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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