MARLIN CONTACT LENS CASE
K-Number: K851497 · 1985-05-16
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Device Summary
Frequently Asked Questions
What is the MARLIN CONTACT LENS CASE?
MARLIN CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1985-05-16. The listed applicant is Marlin Industries. The 510(k) number is K851497.
When did MARLIN CONTACT LENS CASE receive FDA 510(k) clearance?
MARLIN CONTACT LENS CASE received FDA 510(k) clearance on 1985-05-16, under 510(k) number K851497.
Who is the listed applicant for MARLIN CONTACT LENS CASE?
The FDA 510(k) record lists Marlin Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MARLIN CONTACT LENS CASE?
The FDA product code for MARLIN CONTACT LENS CASE is HPX.
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.
Other records listing Marlin Industries 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.
Related Devices (Code: HPX)
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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