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FDA 510(k)

BOSTON CONTACT LENS CASE

K-Number: K951552 · 1995-06-26

Decision Date1995-06-26
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BOSTON CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Polymer Technology Corp.. It received FDA 510(k) clearance on 1995-06-26 under 510(k) number K951552. 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 BOSTON CONTACT LENS CASE?

BOSTON CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1995-06-26. The listed applicant is Polymer Technology Corp.. The 510(k) number is K951552.

When did BOSTON CONTACT LENS CASE receive FDA 510(k) clearance?

BOSTON CONTACT LENS CASE received FDA 510(k) clearance on 1995-06-26, under 510(k) number K951552.

Who is the listed applicant for BOSTON CONTACT LENS CASE?

The FDA 510(k) record lists Polymer Technology Corp. 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 Corp. 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.

View all 23 devices →

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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