BOSTON CONTACT LENS CASE
K-Number: K962512 · 1996-07-12
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Device Summary
Frequently Asked Questions
What is the BOSTON CONTACT LENS CASE?
BOSTON CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1996-07-12. The listed applicant is Polymer Technology Div. Wilmington Partners, L.P.. The 510(k) number is K962512.
When did BOSTON CONTACT LENS CASE receive FDA 510(k) clearance?
BOSTON CONTACT LENS CASE received FDA 510(k) clearance on 1996-07-12, under 510(k) number K962512.
Who is the listed applicant for BOSTON CONTACT LENS CASE?
The FDA 510(k) record lists Polymer Technology Div. Wilmington Partners, L.P. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOSTON CONTACT LENS CASE?
The FDA product code for BOSTON 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.
Other records listing Polymer Technology Div. Wilmington Partners, L.P. 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: 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
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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